Cook Incorporated Patent applications |
Patent application number | Title | Published |
20140277351 | MULTI-STAGE BALLOON CATHETER - A multistage balloon catheter that uses a single lumen to inflate a balloon in stages is disclosed. A fluid port provides fluid communication from an inflation lumen in the balloon catheter to the inner volume of a distal balloon. The distal balloon expands as fluid in delivered to the inner volume of the distal balloon. Once inflated, the pressure continues to rise until a threshold pressure is exceeded. A pressure sensitive inflation valve provides fluid communication into an inner volume of a second balloon disposed at least partially proximal to the distal balloon. The pressure sensitive valve allows fluid communication into the second balloon once the threshold pressure is reached in the first balloon thereby inflating the second balloon. | 09-18-2014 |
20140277069 | VARIABLE LENGTH BALLOON - A variable length balloon catheter assembly and methods for inflating a variable length balloon to a predetermined length. The variable length balloon catheter has a balloon at a distal end and a plurality of stricture mechanisms securing the balloon to the catheter. The stricture mechanisms are provided at known intervals and have a known rupture pressure. The balloon is inflated and a known number of stricture mechanisms are ruptured providing for a variable balloon length based on the number of stricture mechanisms ruptured. | 09-18-2014 |
20130345660 | INTRODUCER TACTILE FEATURE - An introduction system and method of use is provided. The introduction system includes a catheter assembly, a member, and a tactile indicator. The member is configured to be introduced through the catheter assembly and the tactile indicator is configured to provide a tactile sensory input when the member reaches a predetermined position relative to the catheter assembly. As such, the tactile indicator provides increased resistance to the relative motion between the member and catheter assembly when the member reaches the predetermined position. | 12-26-2013 |
20130178790 | INFUSION CATHETER - The disclosure provides an apparatus and methods for removing thrombosis in vessels. The apparatus includes a sheath catheter combined with an aspiration catheter. The sheath catheter includes a first sheath opening in a proximal end of the sheath catheter, a second sheath opening in a distal end of the sheath catheter, a first balloon disposed on an outer surface of the distal end of the sheath catheter, and a passageway extending between the first and second sheath openings. The aspiration catheter is configured to pass through the first and second sheath openings and the passageway of the sheath catheter. The aspiration catheter includes a second balloon, a plurality of infusion ports, and an aspiration port disposed on an outer surface of a distal portion of the aspiration catheter. A relative position between the sheath catheter and the aspiration catheter controls the number of unblocked infusion ports. | 07-11-2013 |
20130103073 | FEMORAL REMOVAL VENA CAVA FILTER - An intravascular filter configured for retrieval through a patient's femoral vein and a method for retrieving the filter through the patient's femoral vein. The filter includes a plurality of struts having connected ends attached together along a longitudinal axis, a shaft disposed along the longitudinal axis and having a first end disposed with the connected ends of the struts, a first cuff slidably disposed on the shaft, and a second cuff disposed over the struts and connected to the first cuff. | 04-25-2013 |
20130035712 | CEREBRAL ANEURYSM CLOSURE DEVICE - The present invention provides a closure device for blocking blood flow into an aneurysm. The closure device includes a frame for positioning the closure device in the aneurysm and a cover supported by the frame to block blood flow through the frame into the aneurysm. The present invention also provides a method of blocking blood flow into an aneurysm using the closure device of the present invention. | 02-07-2013 |
20120222969 | STENT AND METHOD OF FORMING A STENT WITH INTEGRAL BARBS - A method for manufacturing a barbed stent includes providing a sheet of stent material, cutting the sheet to form a stent wire with integral barbs extending therefrom, and forming the stent wire into a final stent shape having a longitudinal axis. A stent for deployment within the body of a patient includes integral barbs. | 09-06-2012 |
20120172908 | VENOUS NITINOL EMBOLIZATION INSERTS - A venous nitinol embolization insert for restricting blood flow includes a tubular member and an embolization material attached to the tubular member. The embolization insert provides a predetermined blood flow rate based on experimental data. A method of controlling restriction of blood flow to a targeted vascular site within a patient's body includes selecting an insert that provides a predetermined blood flow rate corresponding to a desired blood flow rate. The embolization insert is selected from a plurality of embolization inserts that provide varied blood flow rates. | 07-05-2012 |
20120172654 | VENTRICULAR ASSIST DEVICE - A ventricular assist device includes an intravascular blood pump and a collapsible frame. The collapsible frame receives the blood pump therein and is movable between a collapsed state and an expanded state. The collapsible frame engages an interior wall of a body cavity when in the expanded state and is retrievable from the body cavity in the collapsed state. | 07-05-2012 |
20120165789 | Spring Action Wire Guide - A medical wire guide may include a mandrel and a cannula disposed about a portion of the mandrel. A spring may be coupled with the mandrel. The spring may be placed in a loaded state in response to relative displacement between the mandrel and the cannula. Upon release from the loaded state, the spring is configured to bias the mandrel in a distal direction relative to the cannula. | 06-28-2012 |
20120158035 | PUSHABLE COAXIAL BALLOON CATHETER - Coaxial balloon catheters are described herein. The balloon catheter can include outer and inner tubes in a coaxial relationship, with a balloon attached to an end thereof. A support sleeve can be disposed around the inner tubular member proximate the proximal end of the balloon. The support sleeve can have a channel formed therein to communicate with an inflation lumen and a balloon interior. The channel may be formed by separation of two longitudinal edges extending through the support sleeve. The support sleeve can include an outward extending portion that is sized to engage the distal end of the outer tube in order to limit relative movement between the inner and outer tubes. The support sleeve can be configured to orient the inner tube eccentrically or concentrically relative to the outer tube. The support sleeve can have an elongate body that can be extended in proximal or distal direction. | 06-21-2012 |
20120157854 | SYSTEM AND METHOD FOR GAINING PERCUTANEOUS ACCESS TO A BODY LUMEN - Systems and methods for gaining percutaneous access to a body lumen, preferably without a guidewire, are provided herein. The system can include a tubular medical device and a needle with a distal tip. A side port is provided through a wall of the tubular medical device, to be in communication with a distal end opening of the device via a passageway. The needle can be positioned within the side port to extend the distal tip beyond the distal end opening. In this position, the distal tip can form an entry opening in the body lumen, and a distal portion of the device can be advanced over the indwelling needle into the entry opening. The needle can then be withdrawn from the tubular medical device, while maintaining a portion of the tubular medical device in place within the body lumen. | 06-21-2012 |
20120101441 | HINGED CATHETER - The disclosure provides a catheter for positioning in a contralateral femoral approach in highly angulated iliac bifurcations. The catheter comprises an elongate shaft, an adjustable element, and a wire entrance port on the elongate shaft. The elongate shaft has a proximal portion, an intermediate portion, a curved portion, and a distal portion. The curved portion connects the intermediate portion and the distal portion. The adjustable element is configured to encompass the distal portion and the intermediate portion together in a closed position. The adjustable element can be removed away from the distal portion permitting the distal portion in an open position. The wire entrance port is disposed in the intermediate portion near the curved portion. The distal portion is biased to be spaced away from the intermediate portion in the open position. The adjustable element is connected to an operating wire configured to advance and retreat through the wire entrance port. | 04-26-2012 |
20120095542 | INTRALUMINAL MEDICAL DEVICE - A multi-sided intraluminal medical device having a self-expanding frame and a pair of guide bars located on opposite ends of the frame and adapted to enable the frame to be retracted for delivery or retrieval from either end is provided. The intraluminal device may further include a partial or full covering that is circumferentially attached to the frame. Such a medical device may be used as a stent to maintain an open lumen in a vessel (e.g., a vein, artery, or duct), as a valve, or as an occlusion device. | 04-19-2012 |
20120095416 | HEMODIALYSIS CATHETER WITH THROMBUS BLOCKER - A hemodialysis catheter with a plurality of umbrella-like wire members covered with a film which works as a thrombus blocker and can easily and effectively remove the thrombus is disclosed. The hemodialysis catheter has a proximal lumen, the arterial lumen, and a distal lumen, the venous lumen. An elongate member is longitudinally put in either the proximal lumen or the distal lumen, or two elongate members in both lumens. A plurality of umbrella-like wire members are connected to the end of the elongate member. When the hemodialysis catheter is put in the vessel but not in use, the end of the lumen is capped off by the plurality of umbrella-like wire members covered with a film. When it is ready to use, the doctor can pull the elongate member which connects to the plurality of umbrella-like wire members out off the lumen inverting the plurality of umbrella-like wire members and clearing away any thrombus that has formed. | 04-19-2012 |
20120089173 | FILTER WITH MAGNETIC TIP FOR CLOT FRAGMENTATION - A magnetically polarizable, filtering device system and a method of using such a system for capturing embolic material contained within fluid flowing through a body vessel of a patient is provided. The filtering device system generally comprises a source adapted to generate a magnetic field and a filter device adapted to capture embolic material and to unclog itself when necessary or desirable. | 04-12-2012 |
20120083821 | BALLOON WITH INTEGRALLY RETAINED DILATION ELEMENT - A balloon catheter is provided with integral tubular extensions for securing dilation elements to the outside of the balloon. The dilation elements are disposed within the tubular extensions along the working diameter of the balloon. The balloon may be manufactured by extruding a parison and blow molding the parison with the dilation elements installed within the tubular extensions. | 04-05-2012 |
20120078187 | FLEXIBLE INTRODUCER SHEATH - A sheath with improved kink resistance and/or rupture resistance is provided. The sheath includes an inner liner defining a passageway extending longitudinally therethrough. A coil is fitted around at least a part of the inner liner. An outer layer adapted to adhere to the inner liner between the windings of the coil is positioned longitudinally over the coil. Lateral edges can have inwardly curved and outwardly curved portions. Lateral edges can be further structured and arranged to define an asymmetric spacing therebetween. The asymmetric spacing is configured to improve at least one of kink resistance and rupture resistance of the sheath when in a bent configuration. The compressive and tensile strength of the polymer material can be utilized in a manner to inhibit coil segments from sliding along each other or overlapping one another, thereby preventing premature tearing of the material when the sheath is bent. | 03-29-2012 |
20120035586 | Infusion Catheter And Method - An infusion catheter includes an elongate catheter body having a proximal body component and a distal body component. The distal body component includes a distal body outer surface and a distal body inner surface defining an infusion lumen. The distal body component further includes a skeleton, and a porous infusion control textile contacting the skeleton and extending circumferentially about a longitudinal axis of the catheter and defining a fluid emission profile thereof. The porous infusion control textile further includes a fiber network having a higher density space filling configuration at a proximal textile end and a lower density space filling configuration at a distal textile end, and defining a pressure sensitive flow rate property and a pressure insensitive flow distribution property of the fluid emission profile. | 02-09-2012 |
20120035585 | TAPERED VENOUS ACCESS INTRODUCER - A system and method for vessel catheterization is provided, having an introducer sheath and a catheter. The introducer sheath can include a handle and a sheath body extending from the handle. An access lumen is provided in the introducer sheath, and can include a tapered portion that is sized to receive a tapered outer surface of the catheter. The catheter may be a central venous catheter, such as a peripherally inserted central catheter, including a hub, a catheter body with at least one lumen extending distally from the hub, and at least one tube extending proximally from the hub. The introducer sheath is preferably a splittable sheath. The catheter can be inserted into the access lumen, and translated until confronting surfaces of the tapered outer surface of the catheter body and the tapered portion of the introducer sheath contact one another. This arrangement can inhibit buckling and/or kinking of the catheter during insertion, and improve initial catheter tip positioning. | 02-09-2012 |
20120035532 | ASPIRATING AND INJECTING DEVICE - A medical device for aspirating and injecting fluid into a body cavity for use with first and second syringes is provided. The medical device includes an outer needle having an outer lumen formed therethrough. A distal end of the outer needle is configured to puncture tissue for insertion of the needle into the body cavity. An inner cannula is disposed within the outer lumen and has an inner lumen formed therethrough. A distal end of the inner cannula is disposed within the outer lumen. A hub has a first hub opening for fluidly connecting the first syringe to the outer lumen and a second hub opening for fluidly connecting the second syringe to the inner lumen. The inner cannula extends from at least one of the first and second hub openings to the distal end of the inner cannula. A method for treating a cyst is also provided. | 02-09-2012 |
20120016454 | DELIVERY SYSTEM FOR SIMULTANEOUS DEPLOYMENT OF INTRALUMINAL DEVICE - A medical device delivery system includes a retention sheath having a proximal portion and a bi-furcated distal portion having first and second sheath branch portions. The proximal ends of the sheath branch portions are joined together at a sheath branch junction. The system also includes an inner catheter disposed within the retention sheath. The inner catheter includes a proximal portion and a bi-furcated distal portion with first and second catheter branch portions. The proximal ends are joined together at a catheter branch junction. When the sheath is in an initial position, the catheter branch junction is displaced proximally from the sheath branch junction by a distance that is greater than or equal to the larger of a length of a first medical device and the length of a second medical device. | 01-19-2012 |
20110301630 | OCCLUSION DEVICE - An occlusion device having a frame including a plurality of radially expandable struts formed from a plurality of cuts through a tubular wall of a tube. The frame includes a first collar at a proximal end and a second collar disposed in between the proximal and distal ends of the device. A bulbous portion extends between the first and second collars. The bulbous portion includes first and second conical portions joined at their respective bases. A third conical portion extends from the second collar to the distal end of the device. The second conical portion adjacent the second collar and the third conical portion are each defined by a set of cuts forming substantially the same pattern. The first conical portion is defined by a set of cuts forming a pattern that is different from that of the second and third conical portions. The bulbous portion and the third conical portion are configured to expand to approximately the same outer diameter. | 12-08-2011 |
20110295234 | OFFSET SOFT TIP WITH PROPOSED TOOLING - A medical catheter device is disclosed that comprises a tubular shaft member, a soft tip member, and a wire guide lumen extending longitudinally within the tubular shaft member and the soft tip member. The wire guide lumen is offset relative to the centerline within the soft tip member. By offsetting the inner diameter of the soft tip member in such a way as to not change the outward profile of the catheter, the soft tip will have improved tracking across existing stents and eccentric lesions. | 12-01-2011 |
20110288558 | DEPLOYMENT HANDLE FOR AN INTRODUCER - A handle for an implant deployment device converts rotational movement into longitudinal movement in order to provide controlled release of one or more trigger wires. The handle also allows the trigger wire to be withdrawn into the device so that it does not need to be separately removed. A preferred handle includes a rotatable portion ( | 11-24-2011 |
20110288479 | Balloon With Integral Retention of A Dilation Element - A balloon catheter is provided with integral channels for securing dilation elements to the outside of the balloon. The dilation elements have an anchor portion and an intermediate portion that are disposed within first and second longitudinal cavities in the channels. The balloon may be manufactured by extruding a parison and blow molding the parison with the dilation elements installed within the channels. | 11-24-2011 |
20110285059 | Laser Ablation Process For Removing A Portion Of Dilation Element From A Balloon - A method is provided for a ablating dilation beads on a balloon with a laser. The laser removes integral dilation beads from the neck regions and/or the tapered regions of a blow molded balloon. Part of the neck portions of the dilation beads may remain on the body of the balloon after the dilation beads have been removed. | 11-24-2011 |
20110276119 | APPARATUS FOR CURVING AN IMPLANTABLE MEDICAL DEVICE IN A LUMEN - An introducer assembly ( | 11-10-2011 |
20110276022 | Catheter, Fluid Conveying Method, And Percutaneous Procedure - A catheter includes an elongate catheter body having an outer surface with a non-uniform contour and including a plurality of maximum surface elevation points and a plurality of minimum surface elevation points defining a non-uniform elevation profile relative to a longitudinal axis of the catheter body. The outer surface further includes a fluid transfer interface which includes the plurality of minimum surface elevation points and a plurality of porous surface areas, and a tissue contact interface which includes the plurality of maximum surface elevation points and a plurality of nonporous surface areas. The tissue contact interface inhibits external occlusion of the fluid transfer interface during transferring fluid between a fluid lumen defined by the elongate catheter body, and an intraluminal space such as an intravascular space within a patient. | 11-10-2011 |
20110275974 | Clear Flush Check Flow - The disclosure provides apparatus and methods a flow adapter for use with a medical introducer. The flow adapter comprises a housing, a connector disposed on the distal end of the housing, a valve member disposed within the housing, and a side port disposed on the housing. The housing comprises a first opening in a proximal end of the housing, a second opening in a distal end of the housing, and a passageway extending between the first and second openings. The first and second openings and the passageway are configured for the passage of an elongate medical device there through. The connector is in communication with the second opening and is configured for attachment to the medical introducer. The valve member disposed within the housing is configured to prevent the leakage of blood from the adapter. The side port disposed on the housing is configured to be attached to a source of flushing fluid. The side port is fluidly connected to the passageway by one or more conduits extending along a side of the housing and the conduits are configured to direct the flushing fluid to a proximal portion of the passageway adjacent to the first opening. | 11-10-2011 |
20110265826 | METHOD AND SYSTEM FOR CLEANING FLUID RESERVOIR OF VASCULAR ACCESS DEVICE - A method and system for cleaning foreign material from a fluid reservoir of an implantable medical device, the fluid reservoir being substantially enclosed in an interior portion of the implantable device and accessible from an environment exterior of the implantable device through a penetrable septum. An elongated member having a first end and a second end is engaged with a source of ultrasonic energy capable of imparting vibrations to the first end. The septum is penetrated by the elongated member in a manner such that the first end extends into the fluid reservoir, and the second end does not extend into the reservoir. The ultrasonic energy source is activated to impart vibrations into the reservoir via the elongated member first end, in an amount sufficient to break up the foreign material into particulates, which can then be removed from the reservoir. | 11-03-2011 |
20110257674 | VASCULAR OCCLUSION DEVICE - A vascular occlusion device for occluding a body vessel is disclosed. The device comprises a hub having proximal and distal ends and a plurality of anchoring struts. Each anchoring strut has a first end and a second end. The first ends are connected together at the hub. Each of the second ends extends freely from the first end to engage the body vessel for anchoring the device therein. The device further comprises a central strut attached to the proximal end of the hub. The device further comprises a proximal and distal members and an extracellular matrix material. The proximal and distal members are slidibly disposed about the central strut. The extracellular matrix material is disposed about the central strut between the proximal and distal members. | 10-20-2011 |
20110257599 | INTRODUCER SHEATH - Introducer sheath ( | 10-20-2011 |
20110251588 | Infusion Mechanism And Method - An infusion mechanism for treating an intraluminal site in a patient includes an infusion catheter having an elongate body with a proximal body end defining at least one fluid supply orifice, and a distal body end. The elongate body defines a high head loss lumen in fluid communication with a first set of side ports defining a proximal infusion zone. The elongate body further defines a low head loss lumen in fluid communication with a second set of side ports defining a distal infusion zone. | 10-13-2011 |
20110245775 | TAPERED SHEATH - A sheath and a method for making said sheath are provided. The sheath includes with an inner liner defining a passageway about a longitudinal axis extending longitudinally therethrough. A coil is fitted around at least a part of the inner liner. The coil has a series of windings that are locatable at a continuously smaller distance from the longitudinal axis to form a taper in a distal direction. The tube further includes an outer layer positioned longitudinally over the coil that is adapted to adhere to the inner liner. The coil may be spirally wound such that the windings are disposed at a continuously smaller distance from the longitudinal axis in a longitudinal direction. The sheath can have a tapered passageway or a passageway with a uniform diameter. The sheath preferably has a continuous taper along its outer surface from the proximal end to the distal end. | 10-06-2011 |
20110226647 | INTRODUCER ASSEMBLY EXTENSION AND METHOD OF USE - An introducer set includes an introducer and dilator along with an extension in a sealed sterile peal open package. The extension is available for use during procedures where the puncture access site to the patient is close enough to the site to be treated in the patient that the physician's hands and/or head may be positioned in the fluroscopic area while the physician is attempting to maneuver a wire guide to a desired location. When the extension is attached to the introducer, the physician may perform a procedure, such as an antigrade stick in the lower leg of a patient, while maintaining their hands and head outside of the fluroscopic area while direct radiation is being supplied and the wire guide is being maneuvered to a desired treatment location. After the wire guide has been properly positioned and the radiation has been terminated, the extension may be disconnected from the introducer and the remaining portions of the procedure (guide catheter insertion, balloon catheter insertion and dilation, etc.) may proceed in a known manner. The extension need only be in the range of ten to thirty centimeters to allow the physician to work a safe distance from the fluroscopic area undergoing direct radiation. | 09-22-2011 |
20110213303 | Reinforced Catheter Or Sheath With Reduced Friction Surface - A reinforced catheter or sheath includes an inner tube manufactured via an extrusion process from a mixture of thermoplastic and hollow glass beads. The resultant tube exhibits an inner goose bump surface that defines a central lumen. A reinforcement, such as a braid and/or coil is attached to at least a segment of the outer surface of the inner tube. A second tube of thermoplastic is extruded over at least a portion of the reinforcement. The inner goose bump surface exhibits a net low coefficient of friction comparable to that of polytetrafluoroethylene (PTFE). | 09-01-2011 |
20110196479 | COATED IMPLANTABLE MEDICAL DEVICE - A coated implantable medical device includes a structure adapted for introduction into the vascular system, esophagus, trachea, colon, biliary tract, or urinary tract; at least one coating layer posited on one surface of the structure; and at least one layer of a bioactive material posited on at least a portion of the coating layer. Preferably the structure is a stent graft. | 08-11-2011 |
20110196260 | CATHETER ASSEMBLY - A catheter assembly is provided with a flexible tubular body having two lumens. A solid slidable member with a sharp distal end is disposed within one of the lumens. The slidable member is capable of sliding within the lumen of the tubular body between an exposed position in which the sharp distal end of the slidable member protrudes from the distal end of the tubular body and a shielded position in which the distal end of the slidable member is within the tubular body. One advantage is that the sharp distal end of the slidable member may be withdrawn into the tubular body in order to shield a patient from unintentional cutting or irritation from the sharp distal end of the slidable member. | 08-11-2011 |
20110160834 | RAPID EXCHANGE CATHETER - A rapid exchange catheter includes a stiff proximal tube and a relatively flexible tapered distal tube, a guide wire tube being provided in the distal tube, with an aperture for access to the guide wire lumen being provided at the junction between the distal tube and the proximal tube, the tubes being bonded together at their junction. | 06-30-2011 |
20110160756 | Cutting or Scoring Balloon, System and Method of Making a Cutting or Scoring Balloon - A cutting or scoring balloon ( | 06-30-2011 |
20110160755 | Helically Advancing Constriction Crossing Mechanism And Wire Guide Positioning Method For Performing Percutaneous Vascular Procedures - A method of performing a percutaneous vascular procedure includes sliding a vascular constriction crossing mechanism in a proximal to distal direction over a wire guide having a wire guide tip positioned at a proximal side of a vascular constriction, and rotating a sheath of the vascular constriction crossing mechanism about an axis of rotation relative to another sheath of the vascular constriction crossing mechanism. The method further includes advancing a constriction crossing tip by way of helically engaging the sheaths during the steps of rotating, and guiding an intraluminal treatment device into or past the vascular constriction for performing a vascular procedure within the patient. The vascular constriction crossing mechanism includes a first sheath and a second sheath, and a constriction crossing tip coupled with a distal segment of the first sheath. The vascular constriction crossing mechanism further includes a helical coupling between the first and second sheaths, which is configured to convert a torque on one of the sheaths to an axial force on the other of the sheaths for crossing a vascular constriction with the constriction crossing tip. An anchoring mechanism may be coupled with one of the sheaths and includes a deployed state at which the anchoring mechanism contacts a vascular wall of the patient for resisting displacement of the second sheath within a vascular structure of a patient. | 06-30-2011 |
20110160753 | INTRALUMINAL OCCLUSION DEVICES AND METHODS OF BLOCKING THE ENTRY OF FLUID INTO BODILY PASSAGES - An intraluminal occlusion device includes a frame and an attached covering. The frame includes longitudinal struts having concave and convex portions. The intraluminal occlusion devices can be implanted at an opening to a body vessel, such as a blind passage, to block the entry of fluid into the vessel. Methods of blocking the entry of fluid into bodily passages are also described. | 06-30-2011 |
20110160680 | WIRE GUIDE WITH CANNULA - The present invention generally relates to a medical surgical device and specifically a wire guide for percutaneous placement within a body lumen. The wire guide includes an elongated mandrel having sufficient flexibility and kink resistance and a cannula having a stiffness greater than the mandrel stiffness for sufficient pushability. The mandrel extends through the cannula and has a portion extending distal thereto to form a distal tip of the wire guide. The wire guide can further include a slotted cannula to improve the flexibility of the wire guide at the proximal portion of the wire guide. The slots can be arranged in various patterns for increased flexibility along the longitudinal length of the cannula, as well as increased circumferential flexibility along the wire guide. The mandrel may also have a proximally tapered portion to improve the flexibility of the wire guide at the proximal portion of the wire guide. | 06-30-2011 |
20110153007 | Taxane Coatings for Implantable Medical Devices - This disclosure relates to implantable medical devices coated with a taxane therapeutic agent, such as paclitaxel, in one or more solid form(s) having varying dissolution rates. Particularly preferred coatings comprise amorphous and/or solvated solid forms of taxane therapeutic agents that provide durable coatings that release the taxane over a desired period of time, which can be varied in the absence of a polymer by selecting the type and amount of solid forms of the taxane therapeutic agent in the coating. Other preferred embodiments relate to methods of coating medical devices and methods of treatment. The coatings can provide a sustained release of the taxane therapeutic agent within a body vessel without containing a polymer to achieve the desired rate of paclitaxel elution. | 06-23-2011 |
20110152994 | IMPLANTABLE DEVICE - An intracranial stent formed from Nitinol has variable flexibility. The stent ( | 06-23-2011 |
20110152905 | BALLOON WITH SCORING MEMBER - A circumferentially and longitudinally continuous scoring structure having a diameter in an initial unrestrained state that is smaller than a deflated diameter of the balloon is disposed around an outer surface of the balloon in an expanded configuration. The scoring structure continually exerts a radially inward compressive force against the balloon such that when the balloon is expanded from a deflated configuration to an inflated configuration, the scoring structure expands in a radially outward direction and remains in continuous compressive contact with at least a portion of the balloon as the balloon unfolds. The scoring structure may be entirely free of attachment to the balloon and catheter, and may extend substantially a length of a working region of the balloon. The scoring structure may include a plurality of circumferentially compressible members connecting longitudinal members. | 06-23-2011 |
20110152902 | Method For Anchoring Occlusion Plug - A method for occluding a body vessel in a patient to block or reduce blood flow therethrough includes puncturing a blood vessel wall at a proximal vessel entry site with a hollow needle and extending the needle through the proximal entry site into the vessel lumen. The needle is extended through the vessel lumen and extended through the vessel wall at a distal vessel exit site into the extravascular space surrounding the distal vessel exit site. An expandable biocompatible material, such as expandable extracellular matrix (ECM) material, is then ejected though the distal end of the needle into the extravascular space. Then, while continuing to eject the expandable biocompatible plug material, the distal end of the needle is retracted back through the distal vessel exit site into the vessel lumen, such that the plug material continuously extends between the extravascular space surrounding the distal vessel exit site into the vessel lumen. When the plug material is delivered into the lumen of the vessel, the plug material expands, anchoring the plug material to the vessel wall, whereby the plug material forms an occluding plug in the vessel lumen blocking or reducing blood flow therethrough. | 06-23-2011 |
20110152889 | Wound Closure Device - A wound closure device for promoting hemostasis includes a polyhedral body comprising a proximal body end portion and a distal body end portion, including a suture channel horizontally extending through the proximal and distal body end portions, the suture channel containing proximal and distal suture channel openings. An actuator system includes a suture engagement member configured to selectively facilitate axial movement or release of one or more sutures through the channel in an open configuration, and to facilitate securement of suture(s) in the channel in a locked configuration. The proximal body end portion includes a face configured to contact a body surface, anchoring the body to the body surface when suture(s) are secured under tension by the engagement member in the locked position. Once the sutures are secured, the device lends itself to hands-free anchoring until hemostasis is achieved. The device and sutures may then be removed that same day, shortly thereafter. | 06-23-2011 |
20110152760 | Deployment and Dilation With An Expandable Roll Sock Delivery System - An expandable roll sock delivery catheter includes an inner tube, an outer tube having a distal outer tube end, and a medical device, such as a self-expanding stent, collapsibly disposed over the inner tube and concentrically oriented between the inner tube and the outer tube. A hollow tube of expandable balloon material extends from the distal outer tube end, the balloon material being substantially disposed in its entirety within a distal end portion of the outer tube. The balloon material is folded back into the outer tube and over the device as a single layer of balloon material connectively linked to the inner tube proximal to the self-expanding device so as to form an expandable roll sock balloon. The roll sock balloon defines an inflation lumen disposed between the outer tube and inner tube, whereby the inflation lumen is configured for expansion of the roll sock balloon following release of the device. | 06-23-2011 |
20110152715 | BIOPSY NEEDLE WITH VACUUM ASSIST - A surgical cutting device comprises a cannula attached to an actuation mechanism that moves the cannula from a cocked position to a cutting position, a stylet including a distal portion having a sharp distal end, a sample collection region, a vacuum port, and a lumen extending from the vacuum port to the sample collection region such that the sample collection region is in fluid communication with the first vacuum port. When the cannula is in the cocked position, the sample collection region of the stylet is disposed distal of the cannula. The device also includes a fixed volume vacuum source. When cannula is in the cocked position, the vacuum port is not in fluid communication with the fixed volume vacuum source, and when said cannula is in the cutting position, the vacuum port is in fluid communication with the fixed volume vacuum source. | 06-23-2011 |
20110144735 | INTRODUCER - A stent graft introducer ( | 06-16-2011 |
20110144568 | APPARATUS AND METHOD FOR PREPARING FOAM - A device and a method for preparing foam are provided. The device includes a first housing having a first chamber therein and a first movable member positioned at least partially within the first housing. The device also includes a second housing having a second chamber therein, the second chamber being selectively and operably connectable to the first chamber. The second housing further includes a biasing member and a second movable member therein, the biasing member biasing the movable member toward a first end portion of the second housing. The device includes a valve operably connected to the first chamber and the second chamber and movably positionable to selectively control the connection between the first chamber and the second chamber and a handle operably connected to the first movable member and movable to bias the first movable member toward a first end portion of the first housing. | 06-16-2011 |
20110130719 | BALLOON CATHETER - An introducer assembly ( | 06-02-2011 |
20110125249 | Stent Graft and Introducer Assembly - A stent graft ( | 05-26-2011 |
20110125088 | Apparatus for an improved high pressure medicinal dispenser - An apparatus for an improved high pressure medicinal dispenser is disclosed. The high pressure dispenser may include a handle ( | 05-26-2011 |
20110118821 | LOW PROFILE NON-SYMMETRICAL STENT - Various stents and stent-graft systems for treatment of medical conditions are disclosed. In one embodiment, an exemplary stent-graft system may be used for endovascular treatment of a thoracic aortic aneurysm. The stent-graft system may comprise proximal and distal components, each comprising a graft having proximal and distal ends, where upon deployment the proximal and distal components at least partially overlap with one another to provide a fluid passageway therebetween. The proximal component may comprise a proximal stent having a plurality of proximal and distal apices connected by a plurality of generally straight portions, where a radius of curvature of at least one of the proximal apices may be greater than the radius of curvature of at least one of the distal apices. The distal component may comprise a proximal z-stent coupled to the graft, where the proximal end of the graft comprises at least scallop formed therein that generally follows the shape of the proximal z-stent. Further, the distal component may comprise at least one z-stent stent coupled to the distal end of the graft and extending distally therefrom that reduces proximal migration of the distal component. | 05-19-2011 |
20110118816 | Stent Graft and Introducer Assembly - A stent graft ( | 05-19-2011 |
20110114230 | Nickel-Titanium-Rare Earth Alloy and Method of Processing the Alloy - A nickel-titanium-rare earth (Ni—Ti-RE) alloy comprises nickel at a concentration of from about 35 at. % to about 65 at. %, a rare earth element at a concentration of from about 1.5 at. % to about 15 at. %, boron at a concentration of up to about 0.1 at. %, with the balance of the alloy being titanium. In addition to enhanced radiopacity compared to binary Ni—Ti alloys and improved workability, the Ni—Ti-RE alloy preferably exhibits superelastic behavior. A method of processing a Ni—Ti-RE alloy includes providing a nickel-titanium-rare earth alloy comprising nickel at a concentration of from about 35 at. % to about 65 at. %, a rare earth element at a concentration of from about 1.5 at. % to about 15 at. %, the balance being titanium; heating the alloy in a homogenization temperature range below a critical temperature; and forming spheroids of a rare earth-rich second phase in the alloy while in the homogenization temperature range. | 05-19-2011 |
20110071495 | SHAPE MEMORY EMBOLIC PARTICLES HAVING A HIGH PACKING FRACTION - An embolization system having a high packing fraction of embolic particles for use in occluding the flow of body fluid through a body vessel and a method for using such an embolization system are described. The embolic particles, which are made from a shape memory material, exhibit both a collapsed state and an expanded state. The embolic particles exhibit at least a bimodal particle diameter distribution in the collapsed state and expanded state with a particle packing fraction of at least about 0.85. The mixture of embolic particles is delivered into the body vessel in the collapsed state. The particle packing fraction of the mixture in its expanded state causes the occlusion of the flow of body fluid through the body vessel. | 03-24-2011 |
20110066141 | IMPLANTABLE MEDICAL DEVICE HAVING AN ANTI-GASTRIC DISTRESS AGENT - Medical devices, and methods of use therewith, suitable for at least partial implantation within the gastrointestinal portions of a body and having at least one anti-gastric distress agent are provided. The anti-gastric distress agent can include antacids, H2 blockers, proton pump inhibitors, or any combination thereof. The medical device can also include one or more sections having one or more anti-gastric distress agent or antimicrobial agents. The medical device has a length such that when the device is at least partially implanted the first section is accessible to the gastrointestinal portion of the patient's body. A second section having an antimicrobial agent may be external to the gastrointestinal portion. Preferably, device includes a first and second anti-gastric distress agent each having a different controlled release rate. The therapeutic agents can be disposed on one or more surfaces of the medical device and/or impregnated with the material of the medical device. | 03-17-2011 |
20110060275 | Drug Eluting Balloon - There is disclosed a drug eluting balloon catheter assembly provided with a balloon formed of an inner balloon member of non-compliant material and an outer balloon member of a compliant material and which is provided with holes therein for eluting a drug or other fluid. In use, the outer balloon member is biased by contraction onto the inner balloon member thereby keeping the holes therein normally sealed closed and minimizing dead space in the device. | 03-10-2011 |
20110054585 | PROSTHESIS DEPLOYMENT SYSTEM - A trigger wire release mechanism is disclosed that includes a control member for selectively releasing a trigger wire ( | 03-03-2011 |
20110054512 | OCCLUSION DEVICE - An occlusion device ( | 03-03-2011 |
20110054379 | HEMODIALYSIS CATHETER WITH THROMBUS REMOVING DEVICE - The present disclosure provides apparatus and methods for removing thrombus outside of a hemodialysis. The hemodialysis catheter comprises an elongate shaft comprising a plurality of lumens. A first lumen has a first distal port. The first lumen is configured for the flow of a fluid in a first direction. A second lumen has a second distal port proximal to the first distal port. The second lumen is configured for the flow of the fluid in a second direction opposite to the first direction. A third lumen has a third distal port proximal to the second distal port. An elongate device is disposed through the third lumen. The elongate device has an operable member on a distal end or a device to connect to an operable member disposed on the elongate shaft. The operable member is configured to engage and remove thrombus from an exterior surface on the elongate shaft. | 03-03-2011 |
20110046611 | IMPLANT RELEASE MECHANISM - A delivery assembly ( | 02-24-2011 |
20110046610 | OVER-THE-WIRE DETACHMENT MECHANISM - A detachment mechanism, and methods of use, for use in delivering a medical device preferably over a guidewire are provided. The detachment mechanism includes a first and second engagement member. The members are configured to receive the guidewire and have a first end attached to the control member and the device, respectively, a second end, and a notch formed in the body to form an interlocking tooth. The notch is sized to receive the interlocking tooth of the other member. The members are interlockable to couple the medical device to the control member and to allow the guidewire to pass therethrough. The notch can be angled to permit easier detachment between the members and for better torqueability and pushability/pullability between the control member and the medical device. The members can also include a bend region configured to enhance bendability along a portion of the members. | 02-24-2011 |
20110040369 | Implantable Medical Device - A stent graft ( | 02-17-2011 |
20110040368 | MEDICAL DEVICE AND METHOD OF MANUFACTURING SAME | 02-17-2011 |
20110034863 | FLEXIBLE MEDICAL DEVICE FOR CLOT REMOVAL FROM SMALL VESSELS - A medical device and method of applying said medical device to deliver drugs and to remove thrombus or soft tissue clots from vascular or other lumens in a patient is presented. The medical device generally comprises an elongated tubular delivery member having a proximal portion and a distal portion that differ in rigidity and a leak-free connector that is in contact with the proximal portion of the delivery member and is compatible for use with fibrinolytic agents and application of a vacuum. The delivery member includes a metal core made out of multiple shaped-wire strands and a polymer overlay disposed about the core. The wire strands, which have both an A-side and a B-side, are helically wound to form a polygonal shaped lumen whose inner diameter is defined by the A-side of the strands. | 02-10-2011 |
20110034860 | MICRO-NEEDLE ARRAY AND METHOD OF USE THEREOF - A micro-needle array is provided that may be used to deliver a bioactive agent to a therapeutic target. The micro-needle array preferably includes a substrate, a plurality of micro-needles integral with the substrate, and a bioactive agent. At least one micro-needle preferably includes a top surface, a bottom surface, a side surface, and a cavity defined by an inner surface. The bioactive agent may be disposed on the substrate and the plurality of micro-needles. The at least one micro-needle may further include a slit connecting the cavity to an aperture, the slit extending from the top surface to the bottom surface. | 02-10-2011 |
20110022075 | Aspiration Catheter - To prevent a small diameter catheter | 01-27-2011 |
20110022003 | DETACHABLE EMBOLIZATION COIL - An embolization delivery system and a method of using said system by a physician to deliver an embolization coil into the vasculature of a patient is disclosed. The embolization delivery system comprises a delivery tube in the form of a catheter or wire guide that may be reversibly inserted, a delivery catheter placed into the vasculature of a patient, a connector disposed around and permanently coupled to the delivery tube, a detachable embolization coil disposed within a portion of the connector and held in place by compressive forces exerted by the connector, and a release mechanism for detaching the embolization coil. The release mechanism includes a wire with one end being coupled to the catheter, a middle portion being in contact with both the connector and coil, and a second end that may be manipulated in a predetermined manner by the attending physician. The manipulation of the wire splits part of the connector, thereby, reducing the compressive forces exerted by the connector onto the embolization coil and allowing the coil to detach from the embolization delivery system. | 01-27-2011 |
20110009945 | METHOD FOR DEPLOYING A STENT DELIVERY SYSTEM HAVING A BLOWMOLDED HOLDER - A method for deploying a stent delivery system having a blowmolded holder is provided. The stent is configured to expand from a first diameter to a second diameter. The holder is blowmolded to an inner surface of the compressed state. The holder contacts the inner surface and at least portions of side surfaces of the stent, and the holder and the stent have an interference fit therebetween. The deployment method includes delivering the compressed stent placed on the blowmolded holder and the holder into a predetermined deployment side. The deployment method further includes releasing the stent from interference with the holder and expanding the stent from the compressed stent to the expanded stent. | 01-13-2011 |
20110000484 | VASCULAR THERAPY USING NEGATIVE PRESSURE - System and methods for applying vascular therapy to a body vessel using a chamber capable of negative and/or positive pressure relative to ambient are provided. The chamber includes one or more pressure-isolated chambers. A pressure and/or vacuum source is connected to the pressure chamber, and is configured to provide distinct pressures within each pressure-isolated chamber. A controller is coupled to the pressure source, and is configured to control the pressure source such that pressure within each of the pressure-isolated chambers is controlled cyclically to simulate a pulsating pump or peristaltic-like pump action within the body vessel. The use of negative pressure is sequenced such that the resistance to pressure toward the heart is reduced. This effectively “pulls” blood flow toward the heart and creates more space for incoming blood flow. During simulation, medical devices may be introduced to and/or diagnostics may be performed on the targeted vessel. | 01-06-2011 |
20100331817 | THERAPEUTIC AGENT DELIVERY DEVICE WITH A DUAL BALLOON HAVING DISTAL TAPER APERTURES - The present disclosure generally provides a multiple balloon assembly used as part of the distal region of a medical device that is capable of delivering a therapeutic agent into a body vessel having bodily fluid. The multiple balloon assembly comprises an inner balloon and an outer balloon. The outer balloon further comprises a proximal taper region, a middle region, and a distal taper region. The inflation of the inner balloon causes the middle region of the outer balloon to contact the inner wall of the body vessel, thereby, occluding the flow of fluid through the body vessel. The proximal taper region and the distal taper region are configured such that they do not touch the inner wall of the body vessel. One of the distal taper and proximal taper regions has a plurality of apertures configured to allow for the therapeutic agent to be delivered into the body vessel at a predetermined rate. A medical device that incorporates the multiple balloon assembly of the present disclosure, as well as a method for using the medical device and multiple balloon assembly are further disclosed. | 12-30-2010 |
20100323052 | NEEDLE-TO-NEEDLE ELECTROSPINNING - The disclosure relates to a method and apparatus for coating a medical device. The method includes providing an electrospinning apparatus and simultaneously electrospinning at least one solution onto a first surface and an opposing second surface. The apparatus comprises a first spinneret and a second spinneret. An energy source is electrically coupled to the first spinneret and the second spinneret. The first spinneret and second spinneret comprise a reservoir and an orifice fluidly coupled to the reservoir. The first spinneret orifice is located substantially opposite the second spinneret orifice. | 12-23-2010 |
20100318169 | DELIVERY SYSTEM FOR ENDOLUMINAL DEVICES - An introducer or delivery system for introducing implants or medical devices such as embolic protection devices within a patient allows deployment within vessels having a tortuous anatomy. The delivery system includes an actuator wire within the delivery catheter which enables the delivery catheter to be bent near a distal end thereof upon actuation of the actuator wire. | 12-16-2010 |
20100318068 | WIRE GUIDE HAVING DISTAL COUPLING TIP FOR ATTACHMENT TO A PREVIOUSLY INTRODUCED WIRE GUIDE - A coupling wire guide structured to be slidably coupled to a previously introduced wire guide. The coupling wire guide generally includes a main body having a distal end and a coupling tip connection to the distal end. The coupling tip includes a coupling portion defining a coupling passageway having a proximal port and a distal port. A slot is formed in the coupling tip and is in communication with the coupling passageway. The slot extends from the proximal port to the distal port, thereby permitting the coupling wire guide to be “clipped-on” to the mid-section of the previously introduced wire guide or any location having the most efficacy. | 12-16-2010 |
20100316830 | REINFORCING RING - A reinforcing ring ( | 12-16-2010 |
20100312321 | Embolization coil and delivery system - A detachable embolization coil is screw threaded at the proximal end for releasable attachment to a delivery member within a delivery catheter. The coil has a proximal fibred portion and a distal non-fibred portion, the axial length of the non-fibred portion being as great or greater than the axial length of the non-fibred portion. The fibred portion carries a plurality of fibres of thrombogenic fibrous material. In this way, a partially delivered coil may be retracted into a delivery catheter for repositioning, substantially without hindrance from clotting. | 12-09-2010 |
20100298737 | GUIDABLE CUTTING INSTRUMENT - A guidable cutting instrument for cutting a tissue specimen from a tissue mass comprises a cannula having a curve formed along a distal portion thereof, and a stylet having a specimen-receiving notch and a curve formed along a distal portion thereof. The stylet is received in the cannula, and is axially extendable therefrom such that the notch is capable of penetrating the tissue mass. The cannula is axially movable over the extended stylet for severing the specimen from the mass for capture in the notch. The cannula and stylet are each structured and arranged for relative rotation between a first position wherein the cannula curve and the stylet curve are in phase to define a curved condition for a length of the cutting instrument, and a second position wherein the cannula curve or stylet curve is rotated relative to the other curve in a manner to define a generally linear condition of the cutting instrument. The selective relative curvature allows the cutting instrument to be steered around obstructions encountered in the body under real time visualization. | 11-25-2010 |
20100292765 | Apparatus and Method for Cooling the Brain Using a Liquid - Apparatus for cooling the brain comprises a pernasal intubation tube for insertion through one of the nostrils of a patient requiring brain cooling; an inflatable occluder provided the tube for inflation to occlude the nasopharynx of the patient behind the soft palate of the patient thereby to prevent passage of liquid between the nasal cavities and the mouth of the patient; a nostril closure arranged to cooperate with the pernasal intubation tube; an orifice for introduction of a liquid coolant into the nasal cavities; and a liquid vent for insertion in the other nostril of the patient for controlling venting of liquid coolant from the nasal cavities. Also described herein is a method of cooling the brain of a patient in danger of suffering brain damage comprising occluding the air passage leading from the nasal cavities to the mouth cavity of the patient behind the soft palate of the patient and irrigating the nasal cavities of the patient with a coolant liquid. | 11-18-2010 |
20100292726 | THROMBUS RETRIEVAL DEVICE - A thrombus retrieval device has one or more thrombus engaging elements that are movable between a retracted configuration in which they are stowed within the device and a deployed configuration in which they project from the device to snare an adjacent thrombus for removal from a blood vessel. | 11-18-2010 |
20100292614 | MEDICAL SYSTEMS, DEVICES AND METHODS FOR COUPLING WIRE GUIDES - Medical systems, devices and methods are provided for coupling a wire guide to a previously introduced wire guide in intracorporeal procedures, and generally include a supplemental wire guide and a tracking element. The tracking element defines a first passageway and a second passageway. The first passageway is sized to receive the previously introduced wire guide and the second passageway is sized to receive the supplemental wire guide. The supplemental wire guide is attached to the tracking element in a coupled configuration and detached from the tracking element in a decoupled configuration for independent translation of the supplemental wire guide. | 11-18-2010 |
20100286757 | STENT GRAFT - A stent graft | 11-11-2010 |
20100286594 | Device for Treating Hardened Lesions and Method of Use Thereof - A balloon catheter is provided that may be used to dilate hardened regions of a stenosis on a vessel wall. The balloon catheter is provided with cutting elements that extend along a surface of a balloon. At least one bioactive is present, either on the cutting element, within the interior of the balloon, within the material of the balloon or on an outside surface of the balloon. The bioactive is delivered to the vessel wall upon dilation of the balloon. | 11-11-2010 |
20100280586 | MEDICAL DEVICE WITH TENSIONABLY ATTACHED REMODELABLE MATERIAL - Medical devices for implantation in a body vessel, and methods of using and making the same, are provided. A medical device includes a support frame having struts and a weakened frame portion, and a remodelable material tensionably attached to the support frame. The weakened frame portion has a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force. The remodellable material restricts expansion of the frame from a radially compressed configuration to a radially expanded configuration when the weakened frame portion is in the first configuration. The remodelable material can form one or more valve leaflets adapted to regulate fluid flow in a body vessel, such as a vein. | 11-04-2010 |
20100274341 | Introducer Assembly and Method of Manufacturing an Introducer Assembly - An introducer assembly ( | 10-28-2010 |
20100274340 | DEPLOYMENT DEVICE - A stent graft deployment device ( | 10-28-2010 |
20100274277 | EMBOLIC PROTECTION DEVICE WITH MAXIMIZED FLOW-THROUGH - An embolic protection device for capturing emboli during treatment of a lesion in a blood vessel is presented. This embolic protection device generally comprises a plurality of struts having a predetermined shape and being configured to move between an expanded state for engagement with the blood vessel and a collapsed state for filter retrieval and delivery and a filter portion circumferentially attached to the struts having a proximal end and a distal end; the filter portion extending freely from the proximal end to a closed distal end. The filter portion forms at least one annulus chamber in the expanded state with the closed distal end of each chamber being not coincident to the center longitudinal axis of the blood vessel in order capture emboli in the chambers and to reduce any overall restriction of blood flow through the filter portion. | 10-28-2010 |
20100274226 | Deployment Catheter - A catheter for use in an endoluminal delivery assembly includes a device holding region or element on which there is provided a plurality of flexible fingers extending outwardly therefrom. The fingers act to maintain a device to be deployed in the correct position on the catheter and act to resist deformation of the device during deployment. | 10-28-2010 |
20100268244 | STENT INTRODUCER APPARATUS - A dilator element | 10-21-2010 |
20100268243 | FLEXIBLE SHEATH WITH POLYMER COIL - A medical device including a tube having a coil fitted around at least a part of an inner liner, such as PTFE, and a braid extending over at least part of the coil. A polymeric layer is positioned over the braid to adhere to the inner liner. A portion of the coil advantageously comprises a polymer, such as PEEK, while the coil may also have a metal portion. The polymer coil may extend along at least at the proximal region of the tube, and the metal coil may extend along at least at the distal region of the tube. A polymer coil, a metal coil or any combination thereof can extend along the intermediate region of the tube. The polymer coil can be configured so that the tube is longitudinally splittable with a cutting instrument. | 10-21-2010 |
20100262221 | Graft with bioabsorbable support frame - The medical devices, such as stent grafts, described herein preferably include a tubular remodelable graft material attached to a support frame formed at least in part from a metallic bioabsorbable material. The remodelable graft material preferably includes an extracellular matrix material such as small intestinal submucosa (SIS). The support frame attached to the graft is preferably a bioabsorbable magnesium alloy. The devices may be implanted within a peripheral vascular body vessel from a percutaneous delivery catheter. | 10-14-2010 |
20100249899 | PARARENAL STENT GRAFT - A stent graft for endovascular introduction into the pararenal region of the descending aorta. The stent graft has an elongate tubular body ( | 09-30-2010 |
20100249815 | EVERTED SHEATH THROMBECTOMY DEVICE - A medical device for removing a thrombus includes an outer sheath and an inner catheter. The inner catheter is disposed within the inner lumen of the outer sheath. The device also includes a rollsock which is everted upon itself and connected to the distal ends of the outer sheath and inner catheter. A scraping device is attached to the outer surface of the rollsock, such that when the outer sheath is moved relative to the inner catheter the scraping device is exposed to an inner surface of a body vessel. | 09-30-2010 |
20100249654 | WIRE GUIDE - The present invention provides a wire guide ( | 09-30-2010 |
20100241215 | CONFORMABLE STENT STRUCTURE AND METHOD OF MAKING SAME | 09-23-2010 |
20100234878 | CLOSURE DEVICE WITH STRING RETRACTABLE UMBRELLA - A repositionable closure device for occluding a body opening is provided. The closure device includes distal and proximal occluding bodies having expandable distal and proximal umbrella frames. Each umbrella frame includes a plurality of struts connected to a biocompatible sheet material. The distal and proximal umbrella frames expand to expanded configurations on opposite sides of the body opening. The struts of the distal umbrella frame terminate with an eyelet. The distal occluding body is connected to a distal end of a center rod and the proximal umbrella frame is slidable along the center rod via a center ring. At least one drawstring is threaded through the eyelets and the center ring, connecting the distal and proximal occluding bodies. The drawstring extends proximally from the center ring. Manipulation of the drawstring and the center rod is configured to collapse the closure device for at least partial retrieval during repositioning. | 09-16-2010 |
20100234874 | PREFORM AND BALLOON HAVING A NON-UNIFORM THICKNESS - The present invention provides a balloon having a non-uniform thickness that is adapted to facilitate folding of the balloon. The balloon comprises at least one relatively thin section formed between inner and outer surfaces of the balloon, and at least one relatively thick section formed between the inner and outer surfaces. The balloon may be formed from a balloon preform that similarly comprises at least one relatively thin section and at least one relatively thick section. The shape of the balloon preform may be formed, for example, by extrusion. The balloon preform may be placed in a balloon mold having a substantially cylindrical interior surface, and blow-molded to form the finished balloon configuration. The balloon comprises a non-uniform thickness, while comprising a substantially cylindrical outer diameter both after removal from the balloon mold and in an inflated state. | 09-16-2010 |
20100234816 | COATED WIRE GUIDE AND METHOD OF MAKING SAME - In at least one embodiment, a method for making a wire guide is provided. The method comprises applying a polymer coating to a proximal section of a FP coated core wire having a FP coating disposed thereon such that the polymer coating overlays at least a portion of the FP coating. The polymer coating is applied to a distal section of the FP coated core wire having an exposed metal portion such that the polymer coating overlays at least a portion of the exposed metal portion. The polymer coating is removed from the proximal portion of the FP coated core wire to form the wire guide having a proximal portion with the FP coating and a distal portion with the polymer coating. | 09-16-2010 |
20100222862 | Stent, Stent Graft and Other Implantable Assemblies - A stent or other implantable medical device is provided with one or more gripping shoulders which are able, when the stent is compressed onto a delivery cannula to frictionally mechanically engage the outer surface of the catheter so as to grip thereon and maintatin the position of the stent relative to the cannula during withdrawal of the covering sheath. | 09-02-2010 |
20100222805 | METHODS FOR EMBOLIC PROTECTION DURING TREATMENT OF A STENOTIC LESION IN A BODY VESSEL - A method for embolic protection during treatment of a stenotic lesion in a body vessel is provided. The method comprises disposing an embolic protection device in an undeployed state in the body vessel. The device comprises a basket with a set of struts extending from a distal end to a proximal end of the basket, the struts being arranged to define an opening at the distal end, the basket having an expanded state and a collapsed state. A core wire with a distal end and a proximal end is able to reciprocate through the opening at the distal end of the basket. A filter bag is attached only at the distal end of the core wire, the filter bag being located distally to the distal end of the basket when in the collapsed state. The method further comprises moving the core wire relative to the basket to expand the basket and the filter bag in a deployed state downstream from the stenotic lesion to capture emboli during treatment of the stenotic lesion. | 09-02-2010 |
20100217381 | LOW PROFILE SUPPORT FRAME AND RELATED INTRALUMINAL MEDICAL DEVICES - A low profile support frame for use as an or in an expandable intraluminal medical device includes first and second wire members that define arcuate paths having opposing curves. Connectors join the wire members, and barbs can be disposed on the connectors. The support frame has radially compressed and radially expanded configurations. When the support frame is in the radially expanded configuration, substantially no portion of the support frame is disposed on a first transverse axis of the frame opposite one end of the frame and substantially no portion of the frame is disposed on a second transverse axis of the frame opposite the other end of the frame. The support frame can be used as an intraluminal medical device by itself or as a component in a medical device that includes other components, such as a stent, prosthetic valve, occluder, or filter. | 08-26-2010 |
20100211094 | UMBRELLA DISTAL EMBOLIC PROTECTION DEVICE - An embolic protection device for capturing emboli during treatment of a lesion in a blood vessel is presented. This embolic protection device generally comprises a core wire, a plurality of attachment cables and filter struts, and a filter member being configured to move between an expanded state for engagement with the blood vessel and a collapsed state for filter retrieval and delivery. The filter member is circumferentially attached to the attachment cables and filter struts and extends freely from its proximal end to a closed distal end. The core wire is rotated in a first direction to wrap the attachment cables, filter struts, and filter member around the core wire in the collapsed state and is rotated in a second or opposite direction to unwrap the attachment cables, filter struts, and filter member in the expanded state. | 08-19-2010 |
20100211087 | LOOP THROMBECTOMY DEVICE - A thrombectomy device may include an elongate torsion member having a proximal end and a distal end, and a plurality of helically arranged engagement members disposed at a distal portion of the elongate torsion member. Preferably, at least a portion of the engagement members has a rounded, atraumatic shape. The engagement members have a collapsed state where the engagement members are compressed toward the elongate torsion member, and an expanded state where the engagement members are expanded radially outward. Preferably, the engagement members are attached to and extends radially outward from the elongate torsion member at a different longitudinal point such that the engagement members are spaced longitudinally and circumferentially from each other when in the expanded state. When the thrombectomy device is deployed in a body lumen or cavity, the engagement members expands out to contact a wall of the body lumen or cavity. | 08-19-2010 |
20100210995 | SYSTEMS AND METHODS FOR TREATING SUPERFICIAL VENOUS MALFORMATIONS LIKE SPIDER VEINS - Systems and methods treat superficial venous malformations, such as spider veins. The systems and methods distribute a reactive agent, e.g., a light-reactive agent such as talaporfin sodium or verteporfin, at or near an inner wall of a vein. The systems and methods activate the reactive agent by applying energy, e.g. non-thermal light energy at a wavelength that activates the reactive agent to cause localized injury to the inner wall of the vein. | 08-19-2010 |
20100204655 | HEMOSTASIS VALVE SYSTEM - A hemostasis valve system for controlling a flow of fluid includes a housing having a chamber therein, and a valve disposed in the chamber. The valve comprises a plurality of elastomeric valve members, each having opposing shaped first and second faces, a shaped inner edge portion, and a shaped outer edge portion. The valve members are collectively structured and arranged in the valve such that the shaped faces and the shaped inner edges are engaged in interlocking relationship. The valve members have sufficient elasticity to define a yieldable opening along the engaged inner edge portions upon passage therethrough of a medical interventional device. | 08-12-2010 |
20100198328 | Preloaded Stent Graft Delivery Device - A multi-port stent graft delivery device ( | 08-05-2010 |
20100198254 | VASCULAR CLOSURE DEVICE - A device for closure of an opening formed through a wall of a body vessel of a patient is provided, as well as an introducer system for delivery of the closure device. Various embodiments include the closure device having hook members configured to engage the tissue interior of the body vessel wall, hook members configured to engage interstitial tissue adjacent to the body vessel, a plug member to contact sealably the opening from inside the body vessel, and combinations thereof. A retraction member is removably attached to the each of the embodiments to permit manipulation of the device. Remodelable material may be included with each of the embodiments to promote quicker healing. The introducer includes a sheath that is insertable through the opening and a pusher disposed within the lumen of the sheath and movable within the sheath lumen to deploy the device. | 08-05-2010 |
20100181206 | METHOD OF ELECTROPOLISHING MEDICAL IMPLANTS - An electropolishing apparatus and method are provided for polishing stents and other medical implants. The apparatus includes a motor that rotates a roller. The roller continuously rotates the medical implant to be electropolished. One of the advantages of the apparatus and method is that marks generated around the electrical contact between the anode and the medical implant are minimized. In addition, the medical implant is polished more evenly than conventional electropolishing systems. | 07-22-2010 |
20100174361 | PROSTHETIC VALVE WITH SEMI-RIGID AND FLEXIBLE LEAFLETS - The invention relates to a prosthetic valve for regulating fluid flow through a body lumen. The valve includes a frame and a valve member comprising at least one semi-rigid leaflet and at least one flexible leaflet. | 07-08-2010 |
20100174173 | Implantable Medical Device Using Palladium - The present invention provides an improved implantable medical device comprising at least one portion made of a radiopaque material selected from the group consisting of various palladium alloys, including a palladium alloy having, by weight, rhenium in the range of up to about 20 percent, and preferably rhenium at about 14 percent of the alloy, by weight. The present invention further provides a wire guide, an embolization coil, a marker band, a stent, a filter, an RF ablation coil, and an electrode having at least one portion made of the radiopaque material. | 07-08-2010 |
20100168837 | BLOOD PERFUSION DEVICE - Medical devices, as well as methods of treatment and manufacturing such devices, are provided for applying vascular therapy locally within the body vessel. The medical devices include an expandable tubular frame and a sleeve or graft material. The medical devices can be used for local delivery of a therapeutic agent within a body vessel or a tamponade for a lacerated body vessel, while simultaneously allowing perfusion of fluid or blood flow distal of the implanted medical device. The tubular frame of the medical device may have a proximal non-expanding portion and a distal self-expanding support structure. The self-expanding support structure can expand radially outward to urge the graft material to contact the wall of the body vessel. In the expanded configuration, a portion of the device allows fluid flow to continue while the sleeve is against the body vessel wall. | 07-01-2010 |
20100168785 | EMBOLIC PROTECTION DEVICE AND METHOD OF USE - A medical device for embolic protection within a patient's body vessel is provided. The device comprises inner and outer tubular members each having proximal and distal ends and a lumen formed through the proximal and distal ends. A flexible everting filter portion includes a body having a first end attached to the distal end of the inner tubular member and a second end attached to the distal end of the outer tubular member. The inner and outer tubular members are movable relative to one another to position the filter portion within the body vessel. The filter portion is movable from a collapsed, everted delivery and removal configuration to an expanded, generally non-everted deployed configuration. The filter portion expands radially outward to engage the filter body with an enclosing vessel wall. The filter portion allows the passage of blood cells and prevents the passage of emboli or thrombi through the body vessel. | 07-01-2010 |
20100168619 | COMBINATION WIRE GUIDE AND METHOD OF USE THEREOF - The present embodiments generally relate to a medical surgical device and specifically a wire guide for percutaneous placement within a body cavity. The wire guide includes a multi-filar coil having an increasing pitch towards the distal end of the wire guide. Methods of using the device are also provided. | 07-01-2010 |
20100163159 | LARGE DIAMETER DELIVERY CATHETER/SHEATH - A large diameter, flexible, kink-resistant, delivery catheter or sheath for percutaneous delivery of a contained and implantable medical device in the vasculature of a patient. The delivery catheter or sheath includes a reinforcement such as a flat wire coil with uniform spacing between the turns, which is compression fitted about an inner, lubricous PTFE tube. The delivery catheter or sheath further includes an outer tube of a heat formable polyamide material which is heat formed and compressed through the spaces between the turns of the wire coil to mechanically connect to a roughened outer surface of the inner tube. A polymeric radiopaque marker tube may be positioned at the distal end of the coil and between the inner and outer tubes for radiographic visualization. A side port may also be positioned thereat for the infusion of contrast media. | 07-01-2010 |
20100161033 | GRADUALLY SELF-EXPANDING STENT - A gradually self-expanding stent includes a first plurality of stent cells including a first plurality of circumferentially adjacent structural members in mechanical communication with each other. The stent also includes a second plurality of stent cells including a second plurality of circumferentially adjacent structural members in mechanical communication with each other. The circumferentially adjacent structural members of the first and second plurality of stent cells have a compressed configuration and an expanded configuration. A restraining material is attached to each of the circumferentially adjacent structural members defining each of the second plurality of stent cells such that it substantially covers an entirety of each of the second plurality of stent cells in the compressed configuration. Over time, the restraining material releases the structural members defining each of the second plurality of stent cells, thereby allowing the second plurality of stent cells to assume the expanded configuration. | 06-24-2010 |
20100161025 | VARIABLE WEAVE GRAFT WITH METAL STRAND REINFORCEMENT FOR IN SITU FENESTRATION - The disclosure relates to an implantable woven graft for bridging a defect in a main vessel near one or more branch vessels. The graft includes a region of reduced density. Reduced density regions are alignable with at least one of the one or more branch vessels, and are suitable for in situ fenestration, for example by perforation. The disclosed examples are particularly suited for bridging abdominal aortic aneurysms. | 06-24-2010 |
20100160956 | REMOVABLE VENA CAVA FILTER FOR REDUCED TRAUMA IN COLLAPSED CONFIGURATION - The present invention provides a method of capturing thrombi in a blood vessel, which includes delivering a removable filter in a collapsed state within the blood vessel and deploying the filter to an expanded state within the blood vessel. The filter includes a plurality of primary struts and a plurality of secondary struts emanating from a hub and extending arcuately along a longitudinal axis and linearly radially. Each primary strut has an arcuate segment including first and second curved portions. Each secondary strut includes first and second arcs. The primary struts terminate with an anchoring hook. Each primary strut crosses another primary strut along the longitudinal axis in the collapsed state such that the arcuate segments occupy a first diameter and the anchoring hooks occupy a second diameter, the first diameter being greater than the second diameter for filter retrieval or delivery. In the expanded state, the secondary struts centralize the filter in the blood vessel and the anchoring hooks engage with the blood vessel. | 06-24-2010 |
20100160954 | Removable Vena Cava Filter - A removable filter for capturing thrombi in a blood vessel. The filter comprises a plurality of primary struts having first ends connected to each other to define a central axis of the filter. Each primary strut has a curved member extending from the central axis and terminates at an anchoring hook to engage the blood vessel at a first axial plane. The filter further comprises a plurality of secondary struts connected to the curved members of the primary struts and extending therefrom to a free end at a second axial plane to centralize the filter in the blood vessel. | 06-24-2010 |
20100160862 | VARIABLE STIFFNESS INTRODUCER SHEATH WITH TRANSITION ZONE - An introducer sheath includes a lubricious inner liner having a passageway extending longitudinally therethrough, a reinforcing member positioned over the inner liner, and an outer jacket positioned longitudinally over the reinforcing member and the inner liner. The outer jacket has a higher durometer proximal portion, a lower durometer distal portion, and a transition zone between the proximal portion and the distal portion. The transition zone has a variable durometer from a junction with the outer jacket proximal portion to a junction with the outer jacket distal portion, to provide a transition between the higher durometer proximal portion and the lower durometer distal portion. | 06-24-2010 |
20100152698 | ANTI-THROMBOGENIC CATHETER AND METHOD - A medical catheter assembly is provided including an inner catheter member, where that inner catheter member includes a plurality of inner catheter lumens, and an outer sheath with at least one patent sheath lumen. The inner catheter is slidably disposed through a length of the at least one patent sheath lumen in a manner providing a substantially sealing contact between an exterior surface of the inner catheter and an inward surface of the at least one patent sheath lumen. A first of the plurality of inner catheter lumens includes a plurality of apertures to the exterior surface of the inner catheter, and a second of the plurality of inner catheter lumens includes at least one distal end-tip opening. A method of using the assembly is also provided. | 06-17-2010 |
20100152650 | LOADING DEVICE FOR DELIVERING AN EMBOLIZATION COIL INTO A MICROCATHETER - In one embodiment of the present invention, a device for delivering an embolization coil into a microcatheter for deployment of the embolization coil from the microcatheter into a body vessel of a patient is provided. The device comprises a cannula that has a proximal portion extending to a distal portion. The cannula has a lumen formed through the proximal and distal portions. The distal portion has a distal tip that is formed from metal and is configured to interface with the microcatheter for advancing the embolization coil from the lumen into the microcatheter. The proximal portion is at least partially formed of a transparent material for viewing into the lumen to facilitate delivery of the embolization coil into the microcatheter. | 06-17-2010 |
20100148409 | METHOD FOR MANUFACTURING A STENT DELIVERY SYSTEM - A method for manufacturing a stent delivery system having a holder and at least one stent configured to expand from a first diameter to a second diameter is provided. The manufacturing method includes compressing the stent to the first diameter, inserting the stent into a first tube, placing a second tube inside the first tube and inside an inner diameter of the stent. The second tube is airtight. The manufacturing method also includes applying pressure and heat suitable to the second tube, thereby blowmolding the second tube against the stent. | 06-17-2010 |
20100145429 | Introducer sheath and method of manufacture - The present invention relates to a medical device delivery system. The delivery system includes an introducer sheath having an elongated tubular member having a passageway extending generally longitudinally therethrough. The passageway is defined by an inner surface of the tubular member and is configured to receive a medical device moveably disposed therein, where at least a portion of the inner surface of the inner tube comprises a non-uniform surface configured to reduce surface contact between the inner surface and the medical device. The delivery system includes an inner catheter configured to slidably extend throughout the passageway of the introducer sheath. A prosthesis is disposed within a distal portion of the introducer sheath, where the prosthesis is supported within the introducer sheath by the inner catheter. | 06-10-2010 |
20100137966 | SYSTEM AND METHOD FOR SEQUENTIALLY DEPLOYING TWO OR MORE IMPLANTABLE MEDICAL DEVICES - An intraluminal delivery system for sequentially deploying two or more implantable medical devices includes two or more such devices arranged longitudinally adjacent to each other about an inner catheter. One or more separator bands are slideably disposed about the inner catheter, and each of the bands is positioned between adjacent medical devices. An outer catheter, which is proximal to the medical devices, overlies the inner catheter but does not overlie the medical devices. A tubular sheath overlies the outer catheter, the one or more separator bands, and the medical devices. Relative motion between the tubular sheath and the inner catheter allows the medical devices to be sequentially deployed at one or more treatment sites, and relative motion between the inner catheter and the outer catheter allows a distal tip of the inner catheter to be retracted after deployment of each device. | 06-03-2010 |
20100131055 | ARTIFICIAL VALVE PROSTHESIS WITH IMPROVED FLOW DYNAMICS - An expandable venous valve having a support structure configured to enlarge the area adjacent the valve structure. The enlarged pocket areas can be created by forming an artificial sinus adjacent the valve structure in an unsupported section of vessel wall between two support frame sections. | 05-27-2010 |
20100131053 | METHODS OF REDUCING RETROGRADE FLOW - Methods of reducing retrograde fluid flow through a valve within a body vessel are provided. The methods can include the steps of identifying a valve exhibiting an undesirable amount of retrograde fluid flow within a body vessel, such as a venous valve or a heart valve, and providing a means for reducing the retrograde fluid flow. A medical device providing a desired amount of retrograde fluid flow can be modified after permitting the medical device to remain in a body cavity for a remodeling-effective time period. The implanted medical device can be modified by subsequently reducing the amount of retrograde fluid flow permitted across the implanted prosthetic valve within the body vessel. | 05-27-2010 |
20100125327 | EXCHANGEABLE DELIVERY SYSTEM WITH DISTAL PROTECTION - Medical device delivery systems that include a distal protection feature are provided. A distal tip member that includes a distal protection device and a mounting region for a self-expandable, intraluminal medical device is slidably disposed within a passageway defined by a tubular member. | 05-20-2010 |
20100121373 | REMOVABLE VENA CAVA FILTER WITH IMPROVED LEG - A removable filter for capturing thrombi in a blood vessel. The filter has primary struts with first ends attached together along a longitudinal axis. Each primary strut has a body member extending from its first end along the longitudinal axis to an anchoring hook. Each primary strut is configured to move relative to the longitudinal axis between an expanded state and a collapsed state. At least one primary strut has a resistant portion next to the anchoring hook. The resistant portion is configured to contact the blood vessel in the expanded state. The filter also has secondary struts. The secondary struts have proximal ends attached together along the longitudinal axis and distal ends located radially from the longitudinal axis in the expanded state. The secondary struts are configured to engage the blood vessel to centralize the filter in the expanded state in the blood vessel. | 05-13-2010 |
20100114300 | MEDICAL DEVICE WITH LEAK PATH - Medical devices that provide valves for regulating fluid flow through a body vessel are provided. The valves include a support frame having one or more adaptations for forming a leak path between the support frame and an interior wall of a body vessel in which the valve is implanted. A controlled amount of retrograde flow is able to flow through the leak path when the valve is implanted in a body vessel. | 05-06-2010 |
20100114296 | INTRALUMENALLY-IMPLANTABLE FRAMES - Implantable frames for use in body passages are provided herein. The implantable frames can include a plurality of hoop members joined by a plurality of longitudinal connecting members to form a tubular frame defining a cylindrical lumen. The plurality of longitudinal connecting members may include first and second longitudinal connecting members joining a first hoop member to a second hoop member such that the first and second longitudinal connecting members extend across an entire space separating the first and second hoop members. | 05-06-2010 |
20100114294 | Stent Member - A rotationally-symmetric stent graft for deploying in a curved vessel has identical spaced stents along its length, with the stents being further apart in the region of the greatest curvature. The ends of the stents are parallel to each other and to the ends of the graft. The inter-stent spacing may vary along the entire length of the graft or only adjacent one end. | 05-06-2010 |
20100114291 | Introducer for Deploying a Stent Graft in a Curved Lumen and Stent Graft Therefor - A stent graft ( | 05-06-2010 |
20100114290 | Introducer for Deploying a Stent Graft in a Curved Lumen - An introducer ( | 05-06-2010 |
20100106257 | GRAFT PROSTHESIS, MATERIALS AND METHODS - A graft prostheses ( | 04-29-2010 |
20100106256 | GRAFT PROSTHESIS, MATERIALS AND METHODS - A graft prostheses ( | 04-29-2010 |
20100104658 | GRAFT PROSTHESIS, MATERIALS AND METHODS - A graft prostheses ( | 04-29-2010 |
20100104617 | GRAFT PROSTHESIS, MATERIALS AND METHODS - A graft prostheses ( | 04-29-2010 |
20100087844 | MECHANICAL THROMBECTOMY DEVICE - A medical device for removing a thrombus from a blood vessel and a process thereof is presented. The device comprises an outer sheath with a plurality of lumens. A wire guide inserted through one of the lumens is used to place the device proximate to a thrombus. A chemical lysin agent is used to at least partially lyse the thrombus. A wire basket extended through the first lumen proximate to the thrombus is translated back and forth to generate a force that may be transmitted to the partially lysed thrombus assisting in the formation of smaller fragments. A vacuum coupled to the distal end of the second lumen is used to remove the lysed thrombus fragments. | 04-08-2010 |
20100087780 | Wire Guide having Variable Flexibility and Method of Use Thereof - The present invention generally relates to a medical surgical device and specifically a wire guide for percutaneous placement within a body lumen. The flexibility of the wire guide may be varied while it is in place within the body lumen. One embodiment of the wire guide includes and a distal tip positioned at the distal end of the coil. A plurality of core members are positioned side by side within the lumen. Methods of using the wire guide are also provided. | 04-08-2010 |
20100076543 | Multi-strand helical stent - A stent including a stent wire comprising a plurality of filaments twisted into a bundle having a helix, the stent wire bent into a pattern having a plurality of substantially straight wire sections separated by a plurality of bends. The pattern of the stent wire is spirally wound about a central axis in the same direction as the helix formed by the plurality of filaments. Each of the filaments in a bend have a cylindrical cross-section where at least one of the plurality of filaments is displaced and spaced from an immediately adjacent filament in the bend. | 03-25-2010 |
20100069900 | DUAL BALLOON CATHETER ASSEMBLY - A dual balloon catheter assembly and method of use thereof are provided. The dual balloon catheter assembly may be used in a cryoplasty treatment that is provided in combination with eluting an antiproliferative to reduce and/or eliminate vessel fractures, thereby inhibiting proliferative response after angioplasty. | 03-18-2010 |
20100063577 | METHOD OF IMPLANTING A PROSTHETIC VALVE - Methods of implanting a prosthetic valve in a body vessel are provided. A first expandable frame member is delivered to and deployed at a point of treatment in a body vessel. A second expandable frame member is delivered to the point of treatment. The second expandable frame member has an attached graft member that forms a valve adapted to permit fluid flow through the body vessel in a first direction and to substantially prevent fluid flow through the body vessel in a second, opposite direction. After deployment of the first expandable frame member, the second expandable frame member is deployed at the point of treatment such that the second frame member is positioned radially inward of the first frame member within said body vessel to form a prosthetic valve. | 03-11-2010 |
20100063576 | Prosthesis with Moveable Fenestration - An endoluminal prosthesis with a moveable fenestration including a tubular graft body having a proximal end, a distal end, a surface plane at least one fenestration having a perimeter disposed in a sidewall of the tubular body between the proximal end and the distal end, a first biocompatible graft material, and a second biocompatible graft material adjacent to and surrounding the perimeter of the at least one fenestration. The second biocompatible graft material has at least one characteristic different from the first biocompatible graft material and is more flexible than the first biocompatible graft material and is movable relative to the surface plane of the tubular graft body. | 03-11-2010 |
20100063442 | MEDICAL BALLOON HAVING A RESISTANCE TO CIRCUMFERENTIAL TEARING AND METHOD OF PRODUCING THE BALLOON - A medical balloon having a resistance to circumferential tearing comprises a substantially cylindrical portion disposed between first and second tapered portions that have a decreasing cross-sectional area along a length thereof away from the cylindrical portion. The substantially cylindrical portion includes first and second end portions and a midsection disposed therebetween. The midsection includes a first region having a first resistance to tearing and a second region having a second lower resistance to tearing, where the second region extends about only a portion of the circumference of the cylindrical portion and does not extend beyond the midsection. | 03-11-2010 |
20100057201 | PROSTHETIC VALVE WITH VESSEL ENGAGING MEMBER - Medical devices for implantation in a body vessel are provided. Each medical device comprises a main body, a valve, and a vessel engaging member. The vessel engaging member is disposed on an outer surface of the main body. Kits including a plurality of vessel engaging members for use with one or more valve members are also provided. The vessel engaging members have varying radial dimensions, allowing assembly of medical devices having varying radial dimensions. Methods of treating a patient using medical devices according to the invention are also provided. | 03-04-2010 |
20100057185 | Sliding Split-Sleeve Implant Compressor - A system and method for loading an endoprosthesis, such as a stent or valve, into an introducer is provided that permits interventionalists to load the endoprosthesis easily at the bedside. The system can include a compressor for compressing the endoprosthesis to a cross-sectional area less than the cross-sectional area of the introducer lumen. The compressor has a funnel portion at one end where the un-compressed endoprosthesis can be introduced and another end where the introducer and sleeves of a split sleeve device are inserted. The sleeves conform to the compressor passage and surround the endoprosthesis to collapse the endoprosthesis. The split sleeve device also includes a mounting device coupled to the sleeves. The endoprosthesis is compressed and loaded into the introducer by the relative movement of the mounting device and the compressor, where the endoprosthesis remains generally stationary while being compressed and loaded in order to avoid potentially compromising the endoprosthesis. | 03-04-2010 |
20100057184 | INTRALUMINAL SYSTEM FOR RETRIEVING AN IMPLANTABLE MEDICAL DEVICE - An intraluminal system for retrieving an implantable medical device from a body vessel includes, according to one embodiment, a grasping component including at least one deployable arm, where a proximal end of the arm is configured to extend away from a longitudinal axis of the system when deployed, and a first sheath disposed adjacent to the grasping component, where the first sheath includes a radially expandable portion at a distal end thereof. A second sheath overlies the first sheath and the grasping component. Relative motion between the second sheath and the grasping component allows the proximal end of the deployable arm to be deployed for grasping a distal portion of an implantable medical device, and relative motion between the second sheath and the first sheath allows the expandable portion of the first sheath to radially expand to receive a proximal portion of the implantable medical device. | 03-04-2010 |
20100057051 | INTRODUCER SHEATH WITH ENCAPSULATED REINFORCING MEMBER - An introducer sheath and a method for making the sheath. The sheath includes a fluoropolymer liner having a passageway extending longitudinally therethrough. An inner jacket is positioned longitudinally over the liner, and the inner surface of the inner jacket is bonded to the outer surface of the liner. An outer jacket is positioned longitudinally over the inner jacket, and the inner surface of the outer jacket is bonded to the outer surface of the inner jacket. A reinforcing coil is encapsulated within the inner jacket and the outer jacket. | 03-04-2010 |
20100057018 | METHOD OF FORMING AN INTRODUCER SHEATH - A method of forming an introducer sheath having a crease-free tapered distal tip portion. A mandrel is provided having an outer configuration comprising an elongated body and a tapered distal tip portion. A generally tubular inner liner comprising heat shrinkable PTFE, is positioned over the mandrel. The inner liner is heat shrunk to the outer configuration of the mandrel, in a manner that avoids the formation of creases along the inner diameter of the liner. A reinforcing member is positioned over a length of the inner liner, and an outer jacket is positioned over the reinforcing member and the inner liner. The liner, reinforcing member, and outer jacket are heated in a heat shrink enclosure, whereby the outer jacket melts and bonds to an outer surface of the inner liner. | 03-04-2010 |
20100057009 | INTRODUCER FOR USE IN INSERTING A MEDICAL DEVICE INTO A BODY VESSEL AND METHOD FOR SAME - In at least one embodiment of the present invention, an introducer for use in inserting a medical device into a body vessel of a patient is provided. The introducer comprises a housing having a proximal opening, a distal opening and a chamber extending therebetween. A seal in diaphragm form is disposed in the chamber. The seal is formed of polymeric material having a first phase transition temperature higher than about body temperature and a second phase transition temperature that is less than the first phase transition temperature but is greater than about room temperature. The seal is in a first configuration and has an opening formed therethrough when at about room temperature for advancing the medical device through the seal. The seal self-configures to a second configuration when at a temperature of at least the second phase transition temperature for obstructing the body fluid from flowing through the opening of the seal. | 03-04-2010 |
20100057000 | MALECOT WITH TEXTILE COVER - A malecot device includes a textile material covering its deployable malecot wing portion. The textile material is woven in a manner allowing it to be compactly disposed around an undeployed malecot and then expanded to cover malecot wings when those wings are deployed to an expanded outer device diameter. | 03-04-2010 |
20100054075 | VERTEBROPLASTY ALL IN ONE MIXER - In at least one embodiment of the present invention, a device for mixing and dispensing a bone cement mixture is provided. The device comprises an injector housing having a chamber for containing a first and a second bone cement component and a second housing having a chamber for containing a flexible wire mixing element. A plunger actuates within the chamber of the second housing to transfer the wire mixing element to the injector housing for mixing the first and second bone cement components to form the bone cement mixture. The plunger rotates the wire mixing element to mix the bone cement mixture. Thereafter, the wire mixing element is withdrawn from the injector housing and the injector housing is assembled with an injector handle. A plunger coupled to the injector handle advances through the injector chamber to dispense the bone cement mixture from the device. | 03-04-2010 |
20100049171 | DRAINAGE CATHETER AND METHOD FOR CATHETERIZING A PATIENT - In at least one embodiment of the present invention, a drainage catheter for draining part of patient's body is provided. The catheter comprises an elongated member having a proximal portion extending to a distal portion and a lumen formed therethrough for fluid communication with the patient's body. The distal portion is formed of a polymer material having a first phase transition temperature and a second phase transition temperature that is less than the first phase transition temperature but is greater than about body temperature. The distal portion has a first configuration when at about body temperature for at least one of moving and anchoring the distal portion within the patient's body. The distal portion self-configures to a second configuration when at a temperature of at least the second phase transition temperature for retrieval of the distal portion from the patient's body. | 02-25-2010 |
20100049168 | INTRODUCER SHEATH HAVING DUAL REINFORCING ELEMENTS - An introducer sheath for deploying a stent to a target site within a body passageway of a patient. The introducer sheath includes a tubular inner liner having a proximal portion, a distal portion, and an outer surface. A first reinforcing element, and a second reinforcing element are positioned along the outer surface of the inner liner. The first reinforcing element comprises a braid the second reinforcing element comprises a coil. The braid is positioned at the proximal portion of the inner liner and extends distally therefrom. The coil is positioned at the distal portion longitudinally adjacent the braid. The braid has a length that may extend about 90% of the length of the sheath. An outer jacket is positioned longitudinally around the reinforcing elements, and is connected to the inner liner between the respective wires of the braid and the coil. | 02-25-2010 |
20100049167 | INTRODUCER SHEATH HAVING REINFORCED DISTAL TAPER - An introducer sheath has an inner liner having a first length comprising a major diameter, a second length comprising a minor diameter, and a tapered third length axially disposed between the first and second lengths. A coil is positioned over the inner liner and spans at least a portion of each of the first, second, and third lengths. An outer jacket is positioned longitudinally around the reinforcing member and the inner liner, and is bonded to the outer surface of the inner liner. The outer jacket has a first length comprising a major diameter, a second length comprising a minor diameter, and a tapered third length axially disposed between the first and second lengths. The outer diameter first, second, and third lengths substantially correspond to and are disposed radially outwardly of the respective inner liner first, second, and third lengths. | 02-25-2010 |
20100049137 | Device for Crossing Occlusions and Method of Use Thereof - The present invention generally relates to a medical device and specifically to a catheter and wire guide for crossing an occlusion in a body lumen and a method of use thereof. In one embodiment, the catheter includes an incremental positioning mechanism positioned distally of the catheter body. In another embodiment, a lumen containing the wire guide extends through the incremental positioning mechanism and the catheter body. The incremental positioning mechanism allows for adjustment of the axial position of the wire guide relative to the distal end of the catheter body. | 02-25-2010 |
20100049136 | Guide Wire and Method of Use Thereof - The present invention generally relates to a medical device and specifically to a guide wire for reversing the direction of catheterization within a body lumen and to a method of use thereof. In one embodiment, the guide wire includes a first elongated member having a second elongated member attached to the distal end. A spring element joins the distal end of the second elongated member to a third elongated member. The third elongated member is movable between a first position folded upon the second elongated member and a second position extending distally from the second elongated member. | 02-25-2010 |
20100042135 | TEMPORARY FILTER DEVICE - A filter device for capturing thrombi in a body vessel and transformable to a stent to maintain the blood vessel open is disclosed. The filter comprises a plurality of longitudinal struts comprising proximal and distal portions. Each proximal portion has a first end. The first ends are attached together along a longitudinal axis. Each distal portion extends from the proximal portion to an anchoring hook. The distal portions of the longitudinal struts are configured to expand in the body vessel. The device comprises a biodegradable member attached to the device for maintaining the first ends attached together in a closed position. The biodegradable member is comprised of bio-absorbable material so that the biodegradable member degrades at a predetermined time period after the filter is deployed in the body vessel allowing the first ends to radially expand to an open position defining the stent. | 02-18-2010 |
20100042067 | EMBOLIZATION PARTICLES AND METHOD FOR MAKING SAME - In at least one embodiment of the present invention, a method for making embolization particles for occluding fluid flow through a body vessel is provided. The method comprises positioning an elongated body of biocompatible material relative to a cutting device. The elongated body is defined by extrusion of a body cross-section along a longitudinal axis. The elongated body is cut with a cutting device at a plurality of locations along the longitudinal axis to form the embolization particles such that each of the embolization particles has a particle cross-section that corresponds to the body cross-section. | 02-18-2010 |
20100036314 | BALLOON CATHETER AND METHOD FOR MAKING SAME - In at least one embodiment of the present invention a balloon catheter is provided. The balloon catheter comprises a shaft having a lumen formed therethrough. Connected to the shaft is an inflatable balloon. The inflatable balloon has a balloon wall defining a balloon interior surface and a balloon exterior surface that is opposite the interior surface. In fluid communication with the balloon wall is the lumen for inflating the balloon to define an inflated state and for collapsing the balloon to define a deflated state. The balloon wall is textured in the deflated state such that the balloon interior surface is spatially registered with the balloon exterior surface. The balloon in the inflated state is tensioned to have a surface roughness substantially less than a surface roughness of the balloon in the deflated state. | 02-11-2010 |
20100031491 | Method of Incorporating a Tip into an Endovascular Device - An endovascular device tip assembly and method of making the same, incorporating a tip device with a first and second flange, usable with catheters and other suitable endovascular devices is provided. The tip assembly incorporates a tip device by providing a counterbore within a primary bore of a tubular end portion of an endovascular device. The tip device is fitted securely within the counterbore by placing the first flange within the counterbore and the second flange on the outside of the end portion. | 02-11-2010 |
20100023114 | VALVE DEVICE WITH BIASED LEAFLETS - Valve devices useful in the treatment of various valve-related disorders and/or conditions are described. A valve device includes a leaflet and a means for biasing the leaflet in an open configuration. A method of making a valve device comprises the steps of determining a desired closing pressure; determining a desired opening pressure, selecting one or more valve leaflets; selecting an appropriate means for biasing the leaflet in an open configuration based on the determined closing and opening pressures; and attaching the one or more valve leaflets to the means for biasing the leaflet in an open configuration. | 01-28-2010 |
20100023110 | Endoluminal Prosthesis - An endoluminal prosthesis is disclosed and comprises a first generally tubular stent, a second generally tubular stent, and a generally tubular graft member concentrically disposed between the first and second stents. One or more of the first and second stents may have a body portion and a flaring portion. The first and second stents each may have a recoil force such that the combined application of the first and second recoil forces secures the graft member between the first and second stents. | 01-28-2010 |
20100023035 | MULTI-STRANDED APPARATUS FOR TREATING A MEDICAL CONDITION - The present embodiments provide apparatus suitable for treating a medical condition at a target site. In one embodiment, the apparatus comprises a plurality of strands, each having proximal and distal regions, wherein the plurality of strands are twisted in a generally helical manner to form a tubular shape. The proximal and distal regions of each of the plurality of strands comprise a contracted configuration adapted for delivery to the target site. Further, the distal region of at least one of the plurality of strands comprises an expanded, radially deployed configuration adapted to facilitate treatment of the medical condition. The distal region of at least one of the plurality of strands may be deployed in a self-expanding or balloon-expandable manner. | 01-28-2010 |
20100021619 | LOW FRICTION COATED MARKED WIRE GUIDE FOR OVER THE WIRE INSERTION OF A CATHETER - A wire guide includes a mandrel that has a proximal portion and a distal portion. A coating having a low coefficient of friction is disposed on at least part of the proximal portion and the distal portion of the mandrel, where a part of the proximal portion and distal portion of the mandrel without the coating indicates a marking on the wire guide. This marking on the wire guide allows a user to determine a trimmable length of a catheter, and the low friction coating enables the user to easily advance the catheter over the wire guide. | 01-28-2010 |
20100016953 | Anchoring Barb for Attachment to a Medical Prosthesis - Disclosed is an anchoring element for an implantable prosthesis that includes a barb, wherein the anchoring element, which includes a basal portion, comprises a thin layer of material, such as a cannula or sheet of metal, that extends or wraps at least partially around the strut of the prosthesis to which it is attached. The barb is configured to extend outward from the basal portion to penetrate adjacent tissue. The anchoring element is either permanently affixed to the strut, such as by laser or spot welding, crimping, or some other method of bonding, or allowed to slide longitudinally over the strut between two points or stops in order to relieve any excessive loads placed upon the barb that could cause fracture. The anchoring element and strut may be configured to limit axial rotation of the barb, while still allowing longitudinal movement. In another embodiment, the slidable anchoring element may be manipulated following initial deployment to reorient the barb toward the implantation site. | 01-21-2010 |
20100016881 | BIODEGRADABLE FILTER - A medical device that filters thrombi in a body vessel is disclosed. After the need for filtering passes, the device maintains patency in the body vessel without requiring additional steps of percutaneous retrieval or introduction into the patient. | 01-21-2010 |
20100016837 | INTRODUCER SHEATH HAVING A BRAIDED MEMBER AND METHODS OF MANUFACTURE - The present embodiments provide an introducer sheath having a braided member and methods of manufacture. The introducer sheath comprises an inner tube, a braided member disposed over at least a portion of the inner tube, and an outer tube disposed over the inner tube and the braided member. In one embodiment, the braided member comprises a plurality of intersecting first and second wire segments at least partially covered with a coating. At least a portion of the first and second wire segments are bonded together at one or more intersections, for example, by melting the coating, to reduce movement of at least one of the first and second wire segments with respect to one another. Optionally, a coiled member having a plurality of turns may be disposed over a portion of the braided member and the inner tube. | 01-21-2010 |
20100010533 | VARIABLE STRENGTH EMBOLIZATION COIL - An occluding device having variable stiffness for occluding fluid flow through a lumen of a body vessel. The device comprises a wire having a first end and a second end. The wire is formed with a tapered diameter defined by a continuously decreasing diameter from the first end to the second end. The tapered wire is wound into a primary coil having a primary shape. The primary coil may then be wound into a secondary shape or received within a secondary coil which conforms to the primary shape of the primary coil. The tapered diameter provides the device with a continuously decreasing stiffness from a first end to a second end. | 01-14-2010 |
20100010521 | CUTTING BALLOON WITH MOVABLE MEMBER - A balloon catheter and method of use of the balloon catheter are described that may be used to dilate hardened regions of a stenosed region within a body vessel. The balloon catheter is provided with at least one wire that extends between a distal member and a proximal member. The distal member is fixedly attached to the catheter shaft, and the proximal member is slidably disposed along the outer diameter of the shaft. Inflation of the balloon causes the proximal member and the proximal end of the wire attached thereto to distally move along the shaft. Movement of the wire in the distal direction enables subsequent angioplasty to be performed. Deflation of the balloon causes the proximal member and the proximal end of the wire to proximally move along the shaft after completion of the angioplasty procedure. | 01-14-2010 |
20100010499 | HYDRAULIC GUIDEWIRE ADVANCEMENT SYSTEM - A hydraulic guidewire advancement system for enhancing access through lesions or occlusions in distal regions of a patient's vasculature includes a catheter comprising a sheath, a guidewire lumen, and a proximal catheter port connected to a hydraulic driver. A hydraulic guidewire is coaxially disposed through the guidewire lumen, the hydraulic guidewire comprising a piston movably disposed in the guidewire lumen, the piston forming a seal with an interior surface of the sheath. The hydraulic driver is configured to generate hydraulic pressure against the piston sufficient to advance or retract the hydraulic guidewire relative to the catheter. The hydraulic driver can apply positive or negative pressure to the piston, so as to repeatedly contact and break through the lesion with the distal end of the hydraulic guidewire. | 01-14-2010 |
20100010448 | ANCHOR ASSEMBLY - An anchor assembly is used with a medical device to engage the medical device against a body wall. The anchor assembly includes a pivotable anchor and a filament. The anchor is seated in a longitudinal orientation within a recessed channel located at the distal end of the medical device. Pulling on a proximal free end of the filament causes the anchor to pivot from a longitudinal orientation to a perpendicular orientation. The anchor in the perpendicular orientation engages against a body wall to immobilize the medical device. | 01-14-2010 |
20100004672 | OCCLUDING DEVICE FOR OCCLUSION OF A BODY VESSEL AND METHOD FOR MAKING THE SAME - In at least one embodiment of the present invention, a method for making an occluding device for occlusion of fluid flow through a lumen of a body vessel is provided. The method comprises attaching a coating to an embolization coil that is substantially straight. The coating is nominally strained on the substantially straight embolization coil. The embolization coil has a pre-curled tension to facilitate the embolization coil being curled within the lumen of the body vessel when deployed. The embolization coil is restrained from curling until deploying to reduce pre-deployment straining of the coating. | 01-07-2010 |
20100004606 | Deployment assembly and introducer - A deployment assembly ( | 01-07-2010 |
20100004601 | MALECOT GASTRONOMY TUBE WITH SPLITTABLE SHEATH - A gastronomy tube device includes an expandable distal retention portion that is self-expanding. The device includes a removable sheath that circumferentially expands the self-expanding distal retention portion. The distal retention portion preferably is biased into an outer diameter that is greater when released from the sheath than when constrained by it. | 01-07-2010 |
20090319022 | STENT GRAFT - A stent graft ( | 12-24-2009 |
20090319019 | Expandable Tip Delivery System For Endoluminal Prosthesis - An improved delivery system for an implantable medical device includes a retention sheath for an implantable medical device. The retention sheath includes a central lumen extending from a proximal end to a distal end of the retention sheath, and a tapered portion disposed at a distal end of the retention sheath. The tapered portion of the retention sheath includes a first layer made of a low-friction material. The first layer may be movable from a compressed, folded configuration in an initial position, to a substantially uncompressed and unfolded configuration in a deployment position. The retention sheath also includes a second layer made of an expandable material. The second layer is disposed radially outward of and in contact with the first layer, and the second layer is configured to expand in a substantially radially outward direction when the first layer moves from the initial position to the deployment position. | 12-24-2009 |
20090318873 | MEDICAL MALECOT WITH MAGNETS - Embodiments of a malecot device may include magnets configured to maintain a deployed configuration of malecot wings of the device. A malecot device may also include a deployment member that is removably attached thereto. | 12-24-2009 |
20090318870 | BENT OBTURATOR - A catheter-insertion assembly includes a catheter with a proximal end and a distal end, a needle with a proximal end and a beveled distal end forming a sharp distal point, and an obturator with a proximal end and a distal end. The distal end of the obturator includes at least one bend. The bend allows the distal end of the obturator to protect the catheter from the sharp distal point of the needle during insertion of the needle through the catheter. | 12-24-2009 |
20090318854 | GASTRIC PORT SYSTEM - A gastric port system for transport of materials to the interior of a body cavity that may include a port configured to be disposed between a first body cavity and an area adjacent to the first body cavity. The gastric port system may further include a first bolster disposed on the port where the first bolster includes a magnet, and a second bolster disposed on the port where the second bolster includes a magnet, and the magnets are attracted to each other. | 12-24-2009 |
20090312832 | SLIP LAYER DELIVERY CATHETER - A slip layer delivery catheter includes a slip layer delivery catheter includes an outer tube configured with a plurality of strips extending therefrom and terminating in a plurality of distal strip end ends, the plurality of strips defined by empty slotted regions disposed between adjacent strips. An inner tube is coaxially disposed in the outer tube. The inner tube includes a proximal inner tube portion and a distal inner tube portion connected to the distal strip ends. An endoluminal medical device is collapsibly disposed over the inner tube. The plurality of strips is folded back into the outer tube, concentrically orienting the device between the outer tube and the inner tube such that at least a portion of the strips are disposed between the outer tube and the ablumenal device side. | 12-17-2009 |
20090312747 | Wire Guide Having Variable Flexibility and Method of Use Thereof - The present invention generally relates to a medical surgical device and specifically a wire guide for percutaneous placement within a body cavity. The flexibility of the wire guide may be varied while it is in place within the body vessel. | 12-17-2009 |
20090312670 | Wire guide having a rib for coil attachment - The present invention generally relates to a medical surgical device and specifically a wire guide for percutaneous placement within a body cavity. In one embodiment, the wire guide includes an elongated core member having a proximal stop and a distal stop and a rib positioned between the proximal stop and the distal stop. A first coil is positioned over the elongated core member and extends between the proximal stop and the rib. A second coil is positioned over the elongated core member and extends between the rib and the distal stop. | 12-17-2009 |
20090309273 | METHOD OF MAKING A SELF-EXPANDING STENT - A method of making a self-expanding stent includes disposing a stent comprising a shape memory alloy about an inflatable body, and applying a coolant to a surface of the stent. The inflatable body is inflated to radially expand the stent to an expanded diameter from an initial diameter, and the coolant is reapplied to the surface of the stent. The inflatable body is deflated, and the stent is positioned about a mandrel sized to accommodate the expanded diameter of the stent, where the stent reaches a mandrel-defined diameter. The stent is heat set at the mandrel-defined diameter so as to impart a memory of an expanded configuration of the stent to the shape memory alloy. | 12-17-2009 |
20090306678 | DEVICE FOR RETRIEVING A FOREIGN OBJECT LOCATED IN A BODY VESSEL - In at least one embodiment of the present invention, a retrieval device for entrapping and retaining a foreign object located in a body vessel for its extraction therefrom is provided. The device comprises a cage having a proximal end and a distal end and a longitudinal axis extending between the proximal and distal ends. The cage is radially expandable about the longitudinal axis to define an expanded state and to form an opening at the distal end for receiving the foreign object. The cage is collapsible to define a collapsed state and to retain the foreign object therein such that the foreign object is substantially aligned with the longitudinal axis. Extending proximally from the proximal end of the cage is a cable for retrieval of the device in the collapsed state. | 12-10-2009 |
20090299459 | SCORED CATHETER DEVICE - A catheter device including an elongate tubular shaft having a consistent material composition for a substantial proportion of its length. The device includes a proximal shaft portion having a first flexibility and a distal shaft portion having a second flexibility, wherein the second flexibility is greater than the first flexibility and wherein at least the distal shaft portion comprises at least one score in a surface thereof. The device includes a wholly external wire guide structure secured to the tubular shaft by a figure-eight polymer sleeve. | 12-03-2009 |
20090299456 | Delivery system with helical shaft - A delivery system is provided for releasing a medical device within a body cavity. The delivery system may be used in an intravascular procedure to implant a self-expandable stent. A helical structure on the shaft of the delivery system engages the inner surface of the stent. As a result, the stent may be released by rotating the shaft relative to the stent which pushes the stent forward from the distal end of the shaft. | 12-03-2009 |
20090299373 | KYPHOPLASTY BANDED BALLOON CATHETER - A balloon catheter for insertion into a vertebral body is provided. The balloon catheter includes a shaft having a proximal end and a distal end. A lumen extends through the shaft along a longitudinal axis. An inflatable balloon having an uninflated configuration and an inflated configuration is disposed near the distal end of the shaft. The balloon has a proximal portion and a distal portion and an interior and an exterior. The lumen is in fluid communication with the interior of the balloon. An expandable band is wrapped around a section of the exterior of the balloon in a generally proximal-distal direction. The balloon catheter is configured to be positioned within the vertebral body such that the expandable band is configured to prevent leakage of a bone-filling material in a generally lateral direction relative to a vertebral body and facilitate adhesion of the bone-filling material within the vertebral body. | 12-03-2009 |
20090281610 | DELIVERY SYSTEM WITH LOW LONGITUDINAL COMPRESSIBILITY - An improved delivery system for an implantable medical device includes a retention sheath having a proximal end, a distal end, and an inner lumen extending from the proximal end to the distal end. The implantable medical device is disposed within the inner lumen of the retention sheath, which restrains the implantable medical device. A plurality of substantially incompressible rings are disposed within the inner lumen of the retention sheath in a stacked co-axial configuration that extends from the proximal end of the retention sheath in a pre-deployment position to a proximal end of the implantable medical device. Each ring in the plurality of separate rings abuts at least a portion of an adjacent ring. The plurality of separate rings is configured to prevent the implantable medical device from moving toward a proximal end of the retention sheath when the retention sheath is moved from the pre-deployment position to a deployment position. | 11-12-2009 |
20090281564 | Pre-Clot Vessel Dilator - A pre-clot dilator is described that may be used to dilate hardened regions of an occluded region. The pre-clot is provided with one or more struts that extend along a surface of a balloon. Each strut has a proximal fixed end and a distal free end. The distal free end extends past the distal end of the shaft. The distal free end is designed with a penetrating tip that is capable of boring through a proximal portion of the occlusion. Expansion of the balloon allows the strut to pivot about the proximal fixed end of the strut, thereby producing a force sufficient to push out the occlusion towards the vessel wall. The balloon may be deflated so that the strut can collapse over the balloon to create a low profile which enables distal advancement deeper into the occlusion. The procedure is repeated until the occlusion is separated. | 11-12-2009 |
20090281549 | BONE CEMENT MIXING AND DELIVERY DEVICE AND METHOD OF USE - In at least one embodiment of the present invention, a device for mixing and dispensing a bone cement mixture is provided. The device comprises a housing having a chamber configured to contain a first and second bone cement. A plunger including a plunger rod having a piston at a first end and a plunger handle at a second end is configured to actuate within the chamber. A mixing element is disposed adjacent the piston and is configured to rotate within the chamber to mix the first and second bone cement components to form the bone cement mixture. The plunger is configured to rotate the mixing element to mix the bone cement mixture. The plunger is also configured to advance through the chamber. As the plunger is advanced through the chamber, the piston is configured to receive the mixing element and dispense the bone cement mixture from the device. | 11-12-2009 |
20090277385 | METHOD AND APPARATUS FOR COATING INTERIOR SURFACES OF MEDICAL DEVICES - A coating can be applied to an endolumenal wall of a medical device by positioning an optical fiber within the lumen, providing a photo-activated chemical to contact the endolumenal wall, supplying the optical fiber with radiation capable of activating the chemical within the lumen, and withdrawing the optical fiber from the lumen at a controlled rate while the radiation is being emitted from the optical fiber to activate the chemical in close proximity to the endolumenal wall. | 11-12-2009 |
20090276028 | Cartridge Delivery System for Delivery of Medical Devices - A delivery cartridge, delivery system and a method for delivering a medical device are provided. The delivery cartridge includes a housing having a proximal end, a distal end and a cavity defined therein. The delivery cartridge further includes a proximal end covering member connected to the proximal end, a distal end covering member connected to the distal end, and a medical device positioned within the cavity. The housing is adapted to fit within a lumen of a delivery system. | 11-05-2009 |
20090275862 | GUIDEWIRE AND METHOD OF MAKING SAME - In at least one embodiment of the present invention, a method for making a guidewire is provided. The method comprises removing material from a distal portion of a core wire to define a distal tip extending from a proximal portion of the core wire. A collar is positioned adjacent to the distal tip about the proximal portion. | 11-05-2009 |
20090270908 | DEVICE AND METHOD FOR OCCLUSION OF FLUID FLOW THROUGH A BODY VESSEL - The present invention provides an improved occluding device and an improved method of occluding fluid through a body vessel. The occluding device comprises an inner coil. At least one outer coil is disposed about a portion of the inner coil. The outer coil has a pre-curled tension to facilitate the outer coil to be curled within the lumen of the body vessel when deployed. | 10-29-2009 |
20090270841 | Catheters - A catheter arrangement comprises a central tube with a wall of porous material, a proximal portion of which is covered with a non-porous layer. A hub member at the proximal end of the catheter arrangement has a port in fluid communication via the lumen of the central tube with the region surrounding the exposed distal end of the tube. | 10-29-2009 |