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18th week of 2011 patent applcation highlights part 65
Patent application numberTitlePublished
20110106092BONE POSITIONING DEVICE AND METHOD - A method for positioning a bone cut on a bone may involve: coupling a bone cut positioning apparatus with a body bone; adjusting the positioning apparatus in a varus/valgus orientation relative to the body bone; adjusting the positioning apparatus in an anterior/posterior orientation relative to the body bone; and adjusting the positioning apparatus up or down to select a bone resection level.2011-05-05
20110106093PATIENT-SPECIFIC MILL GUIDE - A patient-specific surgical system, such as a patient-specific milling guide, is provided for preparing a bone to receive an orthopedic prosthesis.2011-05-05
20110106094MANDIBULAR DISTRACTION SYSTEM AND METHOD OF USE - A mandibular distraction system and method for treating temporomandibular joint disorders by stretching and relaxing the periarticular muscles of the temporomandibular joint. The system includes a head immobilization device, a patient support device and a facial harness. The system also includes upper and lower mouth guards arranged to fit at least partially around the upper and lower teeth. The mouth guards are configured to operate with a chin strap, sliding assembly, and a displacement device. The displacement device may be actuated to apply force to the facial harness by applying pressure on the chin strap, which is converted by the mouth guards to apply a downward uniform pressure on the back of the jaw, stretching and relaxing the periarticular muscles of the temporomandibular joint. The method of the present invention generally provides steps for allowing distraction of the periarticular muscles to occur while the patient is in a passive, supine position with their mouth closed.2011-05-05
20110106095DRILL GUIDE ASSEMBLY - A drill guide assembly for determining the axis for drilling a bore in a generally dome-shaped bone to receive a component of an orthopaedic joint prosthesis is described. The drill guide assembly includes a drill guide sleeve, a carriage and a platform. The drill guide sleeve is mounted in the carriage towards a first end so that the angular orientation of the drill guide sleeve relative to the carriage can be adjusted about at least one axis. The carriage includes at least one threaded angle-adjustment screw which extends between the carriage and the drill guide sleeve by which the angular orientation of the drill guide sleeve can be adjusted. The platform is fastenable to the bone, and includes at least three feet depending from the platform to engage the surface of the bone with the bone extending towards the platform into the space between the feet.2011-05-05
20110106096Monitoring Thermal Conditions To Vary Operation of an Ultrasonic Needle Tip of a Surgical Instrument - A method and apparatus to operate a surgical instrument in response to a thermal condition being detected that warrants curtailment of further operation. When the thermal condition is reached, command signals are generated that cause a needle of the surgical instrument to either have its vibrational speed slowed, have its vibrational movement stopped, or have it withdrawn from its relative position. The detection is of infrared radiation wavelengths and is carried out with either a thermal imaging device of a thermal recognition device. A corresponding temperature of the detected infrared radiation wavelengths is compared to a critical temperature to determine whether the thermal condition has been reached.2011-05-05
20110106097INTRODUCER ACCESS ASSEMBLY - An elongated introducer access assembly 2011-05-05
20110106098OCCLUSIVE DEVICE DELIVERY SYSTEM - A system for delivering an occlusive device includes a delivery wire assembly configured to be slidably inserted into and through the lumen of a delivery catheter, the delivery wire assembly including a delivery wire conduit defining a conduit lumen and having a conduit distal end forming a first cathode of a position detection circuit, a noble wire disposed in the conduit lumen and having a noble wire distal end forming an anode of the position detection circuit, and a core wire disposed in the conduit lumen and having a core wire distal end, the core wire distal end forming a second cathode of the position detection circuit, wherein an occlusive device is detachably coupled to the core wire distal end.2011-05-05
20110106099LEAD EXTRACTION DEVICE - The disclosure pertains to a lead extraction device which utilizes a chamfered coring tip to separate an implanted object, such as a pacemaker lead, from fibrous tissue and thereby permit the implanted object to be extracted from a body. The lead extraction device features an elongate body having a lead gripping mechanism. The gripping mechanism grips a lead to prevent kinking or simultaneous rotation of the lead with the lead extraction device that may cause tissue damage. The inner lumen of lead extraction device is preferably dimensioned so that a lead will fit within. The lead extraction device is thereby tracked over the lead. The chamfered coring tip on the distal end of the lead separates the lead from fibrous tissue. Through the disclosed lead extraction devices of the present disclosure, the lead may be separated along its length, as well as separated at its distal end from fibrous tissue, thereby permitting the lead to be readily extracted from the body.2011-05-05
20110106100STEERABLE PERCUTANEOUS PADDLE STIMULATION LEAD - The present disclosure relates to a percutaneous paddle stimulation lead that can be steered during implantation. The percutaneous paddle stimulation lead that can be steered in a thickness plane of percutaneous paddle stimulation lead during implantation.2011-05-05
20110106101Steerable Stylet - A stylet for inserting an electrode array into a cochlea includes a first sensor insertable within a lumen of the electrode array and sensitive to force applied by a lumen wall to the first sensor and a first actuator adapted to move the electrode array in response to the force sensed by the first sensor.2011-05-05
20110106102Surgical Instrument and Systems with Integrated Optical Sensor - A surgical instrument has a surgical tool that has a proximal end and a distal end, and an optical sensor that has at least a portion attached to the surgical tool. The surgical tool has a portion that is suitable to provide a reference portion of the surgical tool, and the optical sensor has an end fixed relative to the reference portion of the surgical tool such that the reference portion of the surgical tool can be detected along with tissue that is proximate or in contact with the distal end of the surgical tool while in use.2011-05-05
20110106103HAIR REMOVAL APPARATUS AND CLIP - An apparatus for plucking out hairs of a subject using a thread knots method. The apparatus may comprise at least one pair of pincer-parts hingedly connected through hinged connection; and at least one thread. The pair of hingedly connected pincer-parts creates a structure that is capable of opening and closing when rotated by a user around said rotation mechanism, where the thread is held by the pincer-parts in such a manner that the thread is wrapped around itself creating at least one knot having intersection points. Upon rotating the pincer-parts around the rotation mechanism back and forth in opposite rotation directions, the knots respectively move along a movement-path, where the knots enable capturing the hairs of the subject by tightening around the subject's hairs and plucking them by moving along the movement path, when tightened.2011-05-05
20110106104SNARED SUTURE TRIMMER - A suture trimmer having a shaft, a cutting member, an actuating device, and a snare. The shaft has a first end and a second end and bounds a bore extending from the first end toward the second end. The shaft has an opening formed in a side adjacent the first end. The cutting member is slidably disposed within the bore of the shaft and can be moved between a first position and a second position, such that when disposed in the second position the cutting member closes the opening formed in the side of the shaft. The actuating device is in communication with the cutting member and is operable to move the cutting member from the first position to the second position. The snare extends through the opening and out of the bore at the first end of the shaft.2011-05-05
20110106105Chip-Removing Tool - A cutting insert has the geometry of a tetrahedron with triangle base areas wherein each triangle base area has a tetrahedral frustum as a clamping body for fixing the cutting insert in a tool seat of a carrier tool. Additionally, a tool seat for the cutting insert includes clamping jaws to secure the cutting insert.2011-05-05
20110106106TERMINATION DEVICES AND RELATED METHODS - Devices, methods and kits for forming and/or advancing one or more knots in a tether (e.g., during a tissue modification procedure) are described. In some variations, a tether may be used to gather or compress tissue by bringing two pieces or sections of the tissue together. The tether, which may be under tension, may then be locked to maintain the tension (e.g., by forming one or more knots in the tether). In some variations, an open knot may be advanced along a tether before being converted into a closed knot. The devices, methods and/or kits may be used, for example, in minimally invasive procedures.2011-05-05
20110106107APPARATUS AND METHODS FOR MAINTAINING A FORCE UPON TISSUE USING A LOOP MEMBER - The present embodiments provide apparatus and methods for treating tissue by applying a force to the tissue. In one embodiment, the apparatus comprises a deployable segment having proximal and distal regions, a main body extending therebetween, and a loop member formed at the distal region of the deployable segment. A cannula having a bore is dimensioned to circumferentially surround at least a portion of the main body at a location proximal to the loop member, and a spring member is disposed between the cannula and the loop member. The proximal end of the spring member is affixed to the cannula, and the distal end of the spring member is movable to apply a compressive force to adjust the size of the opening of the loop member and compress tissue disposed within the opening of the loop member. In an alternative embodiment, the cannula is omitted, and a diameter of the loop member is configured to be reduced and increased any number of times before final deployment of the deployable segment.2011-05-05
20110106108DEVICE AND METHOD FOR DELIVERY OF MESH-BASED DEVICES - In some embodiments, a stylet includes a proximal end portion, a distal end portion, and a medial portion between the proximal end portion and the distal end portion. The distal end portion of the stylet is configured to be releasably coupled to a first portion of an implant. The medial portion of the stylet has at least one retention member configured to be releasably coupled to a second portion of the implant.2011-05-05
20110106109PLANAR CLAMPS FOR ANASTOMOSIS - The present embodiments provide medical apparatuses and methods for rapidly forming an anastomosis between two viscera. The medical apparatus generally comprises affixing a clamp to an elongate member. The method generally comprises positioning and then deploying the medical apparatus between and within two stomas via an elongate member.2011-05-05
20110106110DEVICES AND METHODS FOR IMPLANTING A PLURALITY OF DRUG DEPOTS HAVING ONE OR MORE ANCHORING MEMBERS - The present invention is directed to a device for implanting a plurality of drug depots at or near a target tissue site beneath the skin of a patient. The device comprises at least three or more drug depots, wherein each of the at least three or more drug depots has a first surface adapted to receive one or more anchoring members so as to limit movement of the at least three or more drug depots at or near the target tissue site, and wherein at least two of the at least three or more drug depots comprise a second surface adapted to receive the anchoring member after the anchoring member contacts the target tissue site. Each drug depot is capable of releasing a therapeutically effective amount of a drug over a period of at least one day.2011-05-05
20110106111Suture Fixation Arthroscope Apparatus of the Temporomandibular Joint Disk - A suture fixation arthroscope apparatus of the temporomandibular joint (TMJ) disk comprises a first suture needle and a first inner core, a second suture needle and a second inner core, and a third suture needle. The tail ends of the first and second suture needles are connected with a big handle via a valve panel, a vertical groove is opened towards the center of a circle of the surface of the big handle, a horizontal groove which is the same size as the vertical groove is vertically set at the place of the big handle connecting the valve panel. The first inner core includes a seamless tube and a top welded with wire snares, the second inner core includes a seamless tube and a top welded with a crochet hook, the radian near the tails of the first and second inner cores is 90 degrees, a small handle is connected at the tails. The first and second inner cores can pass through the vertical groove of the big handle of the first and second suture needles respectively, the corner of the 90 degrees tail is able to lock rightwards or leftwards at the horizontal groove, the wire snare or the crochet hook at the top of inner cores are able to come out from the top of the suture needles.2011-05-05
20110106112Method And Device For The Fixation Of A Tendon Graft - A fixation device for securing a transplant in a bone tunnel, having a strap with a plurality of protrusions disposed along its length, a fastening member with an aperture therein for passing the strap, and a connection element disposed at a distal end of the strap for engaging a transplant is provided. The fixation device is configured such that, when the distal side of the fastening member lies substantially flush against an outer surface of the bone, a longitudinal axis of the aperture is substantially parallel to a longitudinal axis of the bone tunnel. A method for securing a transplant in a bone tunnel using the aforementioned fixation device is also provided.2011-05-05
20110106113SYSTEM AND METHOD FOR HERNIA MESH FIXATION - The invention includes a surgical fastener and associated deployment system and method that overcomes the drawbacks of prior art surgical mesh fixation devices. The surgical fastener and deployment system may be used to fixate a surgical mesh material to the abdominal wall for the purpose of hernia repair. In accordance with one embodiment, the fastener may include an anchor head comprising a bi-pyramid framework. The anchor head is preferably made from a highly deformable and biocompatible material that withstands high flexural strain within an oscillatory environment. The anchor head may be provided in an elongate, undeployed configuration, and then expanded during deployment into a second, generally planar configuration. The anchor head may be biased to expand into the generally planar configuration from the undeployed configuration in a variety of manners.2011-05-05
20110106114PREFORMED SURGICAL MESH - This invention is related to the medicine branch, more exactly it is related to a prosthetic, preformed, non absorbable or mixed mesh with specific form and size. This is a T-cup mesh or T mesh-cup which is composed by two rectangular attachments with T-cup shape to be used in pelvic or urogynecological surgery in the treatment of: 2011-05-05
20110106115INTRAVASCULAR DEVICE ATTACHMENT SYSTEM HAVING STRUTS - An attachment system for attaching an intravascular device to a vessel wall of a body vessel is disclosed. The attachment system has an intravascular device having a first end and a second end. The intravascular device defines a longitudinal axis along a length thereof. Several struts are connected to one or more ends of the intravascular device. Each strut is configured to move along a strut path relative to the longitudinal axis between an expanded state for engaging the vessel wall and a collapsed state for delivery or retrieval. Each strut has a free end configured to engage the vessel wall in the expanded state.2011-05-05
20110106116APPARATUS AND METHODS FOR ACHIEVING SEROSA-TO-SEROSA CLOSURE OF A BODILY OPENING - The present embodiments provide apparatus and methods for facilitating closure of a bodily opening. In one embodiment, a tissue retraction member and a closure member are provided. The tissue retraction member is advanced in a distal direction through the bodily opening in a contracted state, and then expanded at a location distal to the opening. The tissue retraction member then is proximally retracted to engage first and second serosal tissue regions at least partially surrounding the opening, thereby causing the first and second serosal regions to be disposed in an adjacent relationship. The closure member then is deployed around first and second mucosal tissue regions, such that when deployed, the closure member imposes a compressive force to hold the first serosal tissue region in a sealing relationship against the second serosal tissue region to facilitate sealing of the opening.2011-05-05
20110106117Device and Method for Modifying the Shape of a Body Organ - A tissue shaping device adapted to be deployed in a lumen to modify the shape of target tissue adjacent to the lumen. In one embodiment the device includes first and second anchors; a connector disposed between the first and second anchors; and a focal deflector disposed between the first and second anchors and may be adapted to extend away from the lumen axis and toward the target tissue and/or away from the lumen axis and away from the target tissue when the device is deployed in the lumen. The invention is also a method of modifying target tissue shape. The method includes the steps of providing a tissue shaping device comprising proximal and distal anchors, a connector disposed between the proximal and distal anchors, and a focal deflector; placing the tissue shaping device in a lumen adjacent the target tissue; applying a shaping force from the focal deflector against a lumen wall to modify the shape of the target tissue; and expanding the proximal and distal anchors to anchor the device in the lumen.2011-05-05
20110106118ABSORBABLE VASCULAR ANASTOMOTIC SYSTEM - Provided is an absorbable vascular anastomotic system including an insertion tube of which a front end has a plurality of hooks protruding outward and a rear end has ring-shaped protrusions, and an interlocking tube having grooves corresponding to the protrusions of the insertion tube such that two insertion tubes are inserted into the interlocking tube at both ends of the interlocking tube to be fixed. The insertion tube and the interlocking tube are formed of a material which is absorbed into a living body, and when two insertion tubes into which two blood vessels are respectively inserted to be fixed to the hooks are inserted into the interlocking tube at both ends of the interlocking tube, inner walls of both the blood vessels come into contact with each other in the center of the interlocking tube to be anastomosed. Since the absorbable vascular anastomotic system does not require an additional anastomotic device, it is possible to perform the anastomosis even in a narrow space. Further, since the absorbable vascular anastomotic system is completely absorbed into a living body, it is possible to avoid a risk of foreign body reaction. After the absorbable vascular anastomotic system is completely absorbed, the anastomosed vessels recover their own elasticity.2011-05-05
20110106119ANASTOMOSIS DEVICE - The present invention discloses an microvascular anastomosis device. The device comprises two rotatable and movable ring bodies disposed relatively on a guiding base, and a guiding member lead two vessels to pass through the two ring bodies respectively, wherein a tenon structure is disposed at the two ring bodies for aligning and embedding each other, and inner surface of each vessel is pressured in axial symmetry to make the outer surface of each vessel adhered and fixed onto the inner surface of each ring body, so as not to turn the vessels inside out when performing microvascular Anastomsis.2011-05-05
20110106120INTRAVASCULAR DEVICE ATTACHMENT SYSTEM HAVING TUBULAR EXPANDABLE BODY - An attachment system for attaching an intravascular device to a vessel wall of a body vessel is disclosed. The attachment system includes a tubular expandable body defining a lumen therethrough. The tubular expandable body is configured to move between an expanded state to contact the body vessel and a collapsed state for delivery or retrieval. The tubular expandable body is configured to contact the vessel wall along the length of the tubular expandable body in the expanded state when deployed in the body vessel. An intravascular device is held to the exterior side of the tubular expandable body and is configured to contact the vessel wall when the tubular expandable body is in the expanded state and the system is deployed within a body vessel.2011-05-05
20110106121Hand-held ophthalmic polishing instrument - A surgical instrument and method for polishing or cleaning epithelial cells which reside in the posterior capsule of the eye is provided. The instrument is configured to have a flexible foam tip which is applied to the cells at an angle. This allows the instrument to fully access the posterior capsule and facilitates complete polishing or cleaning of the lens of the eye.2011-05-05
20110106122Modular Scalpel with Retractable Blade - A scalpel (2011-05-05
20110106123TWO-PART SURGICAL DEVICE - A scalpel for performing complex surgeries, such as c-sections, is formed of a body that is preferably elongated and shaped and sized to fit ergonomically into the hands of surgeons. The body has surfaces that are joined to each other by smooth transition elements to insure that the body has no points or sharp edges that could cut or scratch the surgeon or the patient. The body is formed with a triangular notch formed of a beak and an extension. A surgical blade, preferably a standard off-the-shelf surgical blade, is imbedded in the body and the only portion of the blade that is accessible is a portion of its cutting edge spanning the notch. The scalpel is used by introducing the beak into a slit in the tissue with the blade portion facing the direction in which the cut is to be made. The body of the scalpel is then grasped firmly and advanced to make the cut. The initial incision can be made with the tip of the beak. In one embodiment, the body is molded around the blade. in another embodiment, the body is made of two parts that are welded together.2011-05-05
20110106124METHOD AND APPARATUS FOR ARTHROSCOPIC ROTATOR CUFF REPAIR USING TRANSOSSEOUS TUNNELS - There is provided a device for making an arthroscopic rotator cuff repair having a hooked bone-penetrating portion having a sharp tip, a shaft for transmitting force, and a gripping portion. The device may function as a suture passer, being configured to hold or pass one or more suture, and may be cannulated or have an eyelet for this purpose. There is also provided a suture passer of substantially the same shape as the device, which is configured to hold or pass one or more suture, and which may define a channel or have an eyelet for this purpose. Also disclosed herein is a kit comprising the device and suture passer. A method of making a rotator cuff is also disclosed, wherein the greater tuberosity of the humerus is perforated with the device to form a curved bone channel, and a suture is then passed through the bone channel.2011-05-05
20110106125SUGICAL CUTTING ATTACHMENT - A surgical cutting attachment that may include an elongated first member with a proximal end and a distal end including a first blade and an elongated second member with a proximal end and a distal end including a second blade. The second member may be positioned in a side-by-side orientation with the first member and may be connected to the first member at a pivot. A first set of apertures may extend through the first member and a second set of apertures may extend through the second member. A connector may be positioned on the proximal end of at least one of the first and second members. The first and second members may be movable between a first orientation with the first set of apertures aligned with the second set of apertures and the first blade spaced away from the second blade, and a second orientation with the first and second sets of apertures spaced away from each other and the first blade in proximity to the second blade. The first and second blades may form a scissor mechanism and the first and second set of apertures may form a shear mechanism. Methods of using the surgical cutting attachment are also disclosed.2011-05-05
20110106126INSERTER DEVICE INCLUDING ROTOR SUBASSEMBLY - An inserter subassembly including a rotor and drive member such that rotation of the rotor is translated to a linear motion including insertion and refraction paths.2011-05-05
20110106127One Body Lancet and No Pain Type Blood Collecting Device - The present invention concerns a blood withdrawal device comprising a one-piece cap and lancet and a painless impulse generator. The object of the present invention is to withdraw blood painlessly and to reduce a risk of a secondary infection. In order to achieve the object of the present invention, the blood withdrawal device of the present invention comprises a cap, a hollow body and a painless blood withdrawal device. The cap comprises a one-piece cap and lancet within which a lancet is movably combined and a hollow body for a detachable connection with a painless impulse generator or a main body of a blood withdrawal device. The hollow body comprises open ends on both side of the body thereby allowing the lancet to be detachable and the movable axis to be inserted within the body. The painless impulse generator is connected with the main body of the blood withdrawal device through a means for connecting with the main body of the blood withdrawal device defined at one side of the body thereby allowing the movement of the lancet needle and the cap by the movable axis. Therefore painless blood withdrawal is possible.2011-05-05
20110106128DELIVERY WIRE ASSEMBLY FOR OCCLUSIVE DEVICE DELIVERY SYSTEM - A delivery wire assembly for delivering an occlusive device to a location in a patient's vasculature, includes delivery wire conduit defining a conduit lumen, a core wire disposed in the conduit lumen, the core wire having a distal detachment zone, and an enhancing coil disposed around the distal detachment zone, the enhancing coil configured to transfer a distally directed force from the delivery wire assembly to objects located distal of the delivery wire assembly without damaging the distal detachment zone. In one embodiment, the enhancing coil includes a proximal section having a first diameter, a distal section having a diameter larger than the diameter of the proximal section, and a transition section connecting the respective proximal and distal sections, wherein the transition section flares radially in a distal direction.2011-05-05
20110106129Methods and devices to treat obesity - Methods and devices to externally create a restriction on the stomach are described. The devices are contoured to fit the stomach and can be further anchored to the stomach. The degree of deployment of the extragastric restriction device is controllable after implantation. Specialized wires, catheters, ports, and trocars specific for placement of extragastric restriction devices are presented. Systems are described in which adjustability of the devices is provided along with sensing and actuating ability.2011-05-05
20110106130Disposable Gynecologic Instrument For Dilation Of Body Cavities By Fluid Injection - Disposable gynecologic instrument for dilation of body cavities by fluid injection, the construction according to the invention, include the instrument body (2011-05-05
20110106131Systems and Methods for Closing a Percutaneous Vascular Puncture - A system and method for closing a percutaneous vessel puncture at the conclusion of a vascular catheterization procedure includes placement of an intravascular closure device having a tubular membrane mounted about a radially self-expandable scaffold. A tether is attached to a midpoint of the closure device and extends externally therefrom. The closure device is placed by a delivery catheter extending through the puncture site and is radially expanded in a location upstream or downstream of the puncture site. The tether extends through the vessel puncture and tension applied to the tether slides the closure device into a position covering the puncture from within the vessel.2011-05-05
20110106132PARTIAL AORTIC OCCLUSION DEVICES AND METHODS FOR CEREBRAL PERFUSION AUGMENTATION - Methods are provided for partial aortic obstruction for cerebral perfusion augmentation in patients suffering from global or focal cerebral ischemia. Alternatively, the methods can be used to partially obstruct aortic blood flow to condition the spinal cord to secrete neuroprotective agents prior to abdominal aortic aneurysm repair. Partial obstruction of a vessel can be accomplished by a device comprising an elongate catheter and a distally mounted expandable member. The expandable member may comprise one or two balloons. Other medical devices, such as an angioplasty, stent, or atherectomy catheter, can be inserted distal the expandable member to provide therapeutic intervention.2011-05-05
20110106133REMOVEABLE FILTER HEAD2011-05-05
20110106134Indwelling Temporary IVC Filter System with Aspiration - Indwelling temporary inferior vena cava filter systems are disclosed. Such filter systems provide for easy removal of the filter without the need for additional invasive procedures and provide for aspiration of captured emboli. Methods of using such systems for the capture and removal of emboli are described.2011-05-05
20110106135Indwelling Temporary IVC Filter System With Drug Delivery and Aspiration - Indwelling temporary inferior vena cava filter systems are disclosed. Such filter systems provide for easy removal of the filter without the need for additional invasive procedures and provide for dissolution and aspiration of captured emboli. Methods of using such systems for the dissolution, capture and removal of emboli are described.2011-05-05
20110106136IVC Filter With Drug Delivery - Retrievable inferior vena cava filters are disclosed. Such filters provide for easy removal of the filter and provide drug delivery for dissolution of captured emboli. Methods of using such systems for the prevention, capture, dissolution and removal of emboli are described.2011-05-05
20110106137ENDOVASCULAR DEVICE FOR ENTRAPMENT OF PARTICIPATE MATTER AND METHOD FOR USE - A method for filtering particulate matter from a blood vessel in a patient, including inserting a device into the blood vessel, the device including at least an outer structure capable of insertion into the blood vessel; and an inner filter anchored to the outer structure, the inner filter having a one-way valve though which a medical instrument may be passed.2011-05-05
20110106138EXPANDABLE EMBOLI FILTER AND THROMBECTOMY DEVICE - Expandable emboli filter and thrombectomy devices adapted for use with microcatheters to remove debris from blood vessels. The devices embody expanded profiles that span the entirety of various sized target vessels and thus are particularly effective in the engagement of debris found in vessels.2011-05-05
20110106139DEPLOYABLE RECOVERABLE VASCULAR FILTER AND METHODS OF USE - A vascular filter is provided that includes a tubular member having proximal and distal ends, and a guidewire lumen. An expandable frame is attached to the tubular member capable of assuming collapsed and enlarged conditions, and filter material is attached to the frame, the filter material having an open proximal end when the frame assumes its enlarged condition. An apparatus for recovering a vascular filter from a blood vessel is also provided that includes a sheath and a retrieval member deployable from the sheath. The retrieval member includes a connector on its distal end for securing the tubular member, such as an expandable member within a recess for receiving the tubular member. The vascular filter may be constrained in its collapsed condition in a sheath, and the tubular member advanced over a guidewire to a location downstream of a treatment site. The vascular filter is deployed and expanded to its enlarged condition across the blood vessel, the guidewire remaining in place. A procedure is performed at the treatment site, the vascular filter capturing released emboli. The retrieval device is advanced over the guidewire, the vascular filter is secured to the retrieval member, and the vascular filter and retrieval device are withdrawn from the blood vessel.2011-05-05
20110106140VERTICAL AND HORIZONTAL NASAL SPLINTS AND METHODS OF USE - A nasal opening device. The nasal opening device includes a vertical splint configured to extend from an upper portion of a nose to a lower level of nasal bones and a horizontal splint configured to extend from a first lateral wall to a second lateral wall of a nose. A vertical flexible member is integrated with said vertical splint and positioned such that upon attachment of the vertical splint to a nose the flexible member is adjacent to a nose tip and assists with maintaining a nose tip in an elevated position, said vertical splint having an adhesive layer for attachment to a nose. A flexible member is integrated with said horizontal splint and extends from said first lateral wall to said second lateral wall of a nose.2011-05-05
20110106141ROBOT SYSTEM FOR ENDOSCOPIC TREATMENT - A robot system for endoscopic treatment includes a gripping unit, a manipulator unit, a treatment instrument drive unit, a gripping force detection unit, a control unit. The gripping unit is inserted into a body cavity along with an endoscopic apparatus and grips desired living tissue using gripping members. The manipulator unit includes a multi-joint structure that enables bending and stretching. The treatment instrument drive unit pulls and pays out wires. The gripping force detection unit detects gripping force provided by the gripping members. The control unit instructs the treatment instrument drive unit to pull and pay out the wires for the gripping operation so that the gripping force detected by the gripping force detection unit falls within a predetermined range when the gripping unit in the gripping state moves.2011-05-05
20110106142SUTURING INSTRUMENTS AND SUTURING SYSTEMS - A needle storage and disposal cartridge is loaded with a needle receptor, and or suture and needle. By insertion of a forceps arm into the cartridge the needle receptor can be affixed to an arm of the forceps, and similarly removed after use. The forceps may conveniently be used for gripping and retaining a needle during suturing. A number of alternative suturing forceps and needle receptors are disclosed.2011-05-05
20110106143MEDICAL INSTRUMENT - A medical instrument includes a handle on the proximal end and a shank rotatably arranged on the handle. A tool is arranged on the distal end of the shank. This tool is rotatable relative to the shank. An actuation element is arranged on the handle. The actuation element may be moved into at least two switch positions, wherein in a first switch position the actuation element is coupled in movement to the shank and in a second switch position the actuation element is coupled in movement to the tool.2011-05-05
20110106144Surgical instrument - In order to provide a surgical instrument which is particularly simple to manipulate and enables force to be transmitted particularly directly to at least two tool elements wherein the surgical instrument comprises said at least two tool elements which are movable relative to one another and are arranged at a distal end of a guide device of a surgical instrument, and also comprises a force transmission device for transferring an actuating force from a proximal end of the force transmission device to a distal end of the force transmission device for the purposes of moving at least one of the at least two tool elements relative to the guide device, it is proposed that the surgical instrument should comprise a coupling device for selectively coupling the force transmission device directly or indirectly to at least one of the at least two tool elements.2011-05-05
20110106145TOOL FOR MINIMALLY INVASIVE SURGERY - The present invention relates to an easy-to-control tool for minimally invasive surgery. In accordance with an aspect of the present invention, there is provided a tool for minimally invasive surgery comprising, an elongated shaft having a predetermined length, an adjustment handle manually controllable by a user, a first pitch axis part and a first yaw axis part positioned around one end of the elongated shaft for transferring motions in pitch and yaw directions following the operation of the adjustment handle, a second pitch axis part and a second yaw axis part positioned around the other end of the elongated shaft for operating corresponding to the operations from the first pitch axis part and the first yaw axis part, respectively, and an end effector controllable by the second pitch axis part and the second yaw axis part, wherein the first pitch axis part drives the second pitch axis part by at least one pitch axis actuating cable, and the first yaw axis part drives the second yaw axis part by at least one yaw axis actuating cable.2011-05-05
20110106146TOOL FOR MINIMALLY INVASIVE SURGERY - The present invention relates to an easy-to-control tool for minimally invasive surgery. In accordance with an aspect of the present invention, there is provided a tool for minimally invasive surgery comprising, an elongated shaft having a predetermined length, an adjustment handle manually controllable by a user, a pitch direction handling part and a yaw direction handling part positioned around one end of the elongated shaft for transferring motions in pitch and yaw directions following the actuation of the adjustment handle, a pitch direction actuating part and a yaw direction actuating part positioned around the other end of the elongated shaft for operating corresponding to the operations from the pitch direction handling part and the yaw direction handling part, respectively, an end effector controllable by the pitch direction actuating part and the yaw direction actuating part, and a plurality of cables for transferring the from the pitch direction handling part and the yaw direction handling part to the pitch direction actuating part and the yaw direction actuating part, respectively.2011-05-05
20110106147Percutaneous puncture sealing system - A method of sealing percutaneous punctures in a patient's body that open into an internal body cavity using a sealing material such as a fibrin adhesive while preventing the sealing material from entering the body cavity. An apparatus for delivering the sealing material is also disclosed.2011-05-05
20110106148CLOSURE SYSTEM AND METHODS OF USE - A closure system and methods of use are provided for use in sealing an opening in a body tissue, such as a vascular puncture site. A method of closing the opening in the body tissue can be performed with the closure system having a closure clip. The method can include positioning the closure clip in a first closure clip position adjacent to the opening in the body tissue such that a plurality of spikes of the closure clip are inserted into the tissue at a location outward from a central axis of the opening. Subsequently, the closure clip can be positioned in a second closure clip position such that the plurality of spikes are pulled inward toward the central axis of the opening so as to pull the tissue between the opening and each of the spikes together and close the opening.2011-05-05
20110106149SEPTAL OCCLUDER AND ASSOCIATED METHODS - Devices are provided for closing septal defects such as PFOs. The devices generally include a proximal anchor member, a distal anchor member, and a flexible center joint connecting the two anchor members.2011-05-05
20110106150Surgical Method Utilizing a Soft-Tipped Anvil - A surgical method for treating a tissue structure having a wall and a lumen may include providing a substantially rigid anvil and a flexible tip affixed to and extending from the distal end of that anvil; making an incision in the wall of the tissue structure; inserting the flexible tip and at least a portion of the rigid anvil through the incision into the lumen of the tissue structure; and deforming at least one connector, introduced from outside the wall of the tissue structure, against the portion of the rigid anvil located within the lumen of the tissue structure.2011-05-05
20110106151SQUARE LOCK SUTURE KNOT - A method for forming a suture knot, the method comprising: 2011-05-05
20110106152APPARATUS AND METHOD FOR FORMING SELF-RETAINING SUTURES - An apparatus and method for cutting retainers on a continuous strand is provided. The apparatus may include a rotary head member configured to be rotatably driven about a longitudinal axis. The rotary head member may include a center hole substantially coincident with the longitudinal axis and configured to receive the strand. A retainer forming member may be supported on the rotary head member and may include a cutting edge directed substantially inward toward the longitudinal axis. When the rotary head member rotates about the longitudinal axis and the strand is continuously pulled through the center hole along the longitudinal axis, the cutting edge may intermittently or continuously cuts retainers about an outer surface of the strand.2011-05-05
20110106153Method and Apparatus for Sternal Closure - A method and apparatus for securing a fractured or sectioned sternum in a patient's body is disclosed. The apparatus can include an attachment member and an adjustable flexible member construct. The attachment member can have a flexible member holder. The adjustable flexible member construct can have first and second ends and a body defining at least one passage portion. The first and second ends can be passed into and through the at least one passage portion via first and second openings associated with the at least one passage portion of the adjustable flexible member construct to form a pair of loops. The attachment member can be configured to be coupled to at least one of the formed pair of loops. The adjustable flexible member construct can be positioned about the sternum and can be reduced to compress the fractured or sectioned sternum.2011-05-05
20110106154PARTIAL THICKNESS ROTATOR CUFF REPAIR SYSTEM AND METHOD - A suture anchor is disclosed which has an elongated body having a distal end, a proximal end and an exterior surface. An axially oriented bore extends into the body from the proximal end and a proximal portion of the bore has a plurality of abutment surfaces for engaging a tool. The bore includes one or more axially oriented suture passages leading to a suture attachment within the bore. A length of suture extends into the at least one suture passage from the body proximal end and extends to the suture attachment. A screw thread spirals about a portion of the exterior surface of the body adjacent the at least one suture passage. Between the bore and the exterior surface of the body the body has a wall thickness and wherein the suture passage comprises the area where the wall thickness goes to zero.2011-05-05
20110106155EXTERNAL RETENTION MECHANISM FOR SUTURE ANCHOR - Among other things, embodiments of a retaining mechanism for holding a portion of the suture of a suture anchor are disclosed. When a suture anchor is inserted into a patient, the portion of the suture extending from the body is held in tension by a two-piece snap-fit mechanism. One piece has a base with an extending shaft portion and a bulbous head, and a lumen runs through the shaft. The second piece has a hole or space for snapping the second piece onto the first piece. The extending portion of the suture runs through the lumen in the first piece and can be wrapped around the shaft. Snapping the second piece onto the first contains the suture and prevents loss of tension in it.2011-05-05
20110106156PACIFIER AND FEEDING DEVICE - Disclosed is a combined pacifier and spoon device comprising a handle attached to a sucking body. The sucking body comprises a posterior region proximal to the handle and an anterior end distal to the handle. A curved upper side of the sucking body defines a recess extending at least part way between the posterior region and the anterior end thereof thereby forming a spoon for feeding food to a person with the recess for holding the food.2011-05-05
20110106157Self-Locking Interference Bone Screw for use with Spinal Implant - The present invention is generally directed to a unique bone screw which, in one form, may be used to engage with and attach an implant to bone or bony tissue. In one embodiment, a bone screw includes an elongate shank extending along a longitudinal axis from an enlarged proximal head portion to a distal tip. The elongate shank includes a first portion having a first non-tapered, linear external profile and a second portion having a first tapered external profile that increases toward the proximal head portion. The second portion is positioned between the first portion and the head portion and terminates distally of the proximal head portion. In one form of this embodiment, the bone screw can be advanced through a passage of an implant such that an interference fit is provided between the bone screw and the implant.2011-05-05
20110106158SYSTEM FOR STABILIZING A PORTION OF THE SPINE - A system for stabilizing a portion of the spine comprising an elongate plate attached to one or more vertebrae by a number of bone anchors, with the system including one or more features that provide visualization of an implant disposed within a vertebral space and/or the interface between the implant and the adjacent vertebral tissue. A holding instrument is included that is engageable to the plate for positioning the plate adjacent the spinal column.2011-05-05
20110106159SPINAL FIXATION PLATE ASSEMBLY - A spinal fixation plate has inner and outer surfaces through which a pair of adjacent screw holes extend along generally parallel axii. The screw holes accommodate the heads of conventional bone screws while allowing the threaded shafts of the screws to pass therethrough. A recess extends into each screw hole for receiving a V-shaped latch having a pair of wings joined to a head via elastically deformable arms. The latch is moveable between a deployed position in which the wings extend into the screw holes to prevent a screw seated therein from backing out and a retracted position in which the wings arc retracted from the screw holes enabling the screws to be backed out of the plate.2011-05-05
20110106160SYSTEMS AND METHODS FOR POSTERIOR DYNAMIC STABILIZATION OF THE SPINE - Devices, systems and methods for dynamically stabilizing the spine are provided. The devices include an expandable spacer having an undeployed configuration and a deployed configuration, wherein the spacer has axial and radial dimensions for positioning between the spinous processes of adjacent vertebrae. The systems include one or more spacers and a mechanical actuation means for delivering and deploying the spacer. The methods involve the implantation of one or more spacers within the interspinous space.2011-05-05
20110106161Position Retaining Crosslink - A crosslink for a spinal stabilization system is disclosed that provides significant increased torsional stability for the spinal stabilization system. The crosslink includes a first crosslink arm and a second crosslink arm having an eye. An eyebolt is included that has a horizontal passageway for receiving at least a portion of the first crosslink arm and an upper portion for receiving the eye of the second crosslink arm. The eyebolt includes a means for inhibiting rotational and translational movement of the portion of the first crosslink arm.2011-05-05
20110106162Composite Connecting Elements for Spinal Stabilization Systems - Elongated connecting elements include bodies having composite cross-sections defined by a center core that is surrounded by an outer portion. The center core includes a first material and the outer portion includes a second material that is distinct from the first material. In one particular form, a connecting element includes a maximum dimension across an outer cross-sectional shape of the outer portion that is less than a minimum dimension across an oblong or round outer cross-sectional shape of a polyetheretherketone (PEEK) connecting element, and the connecting element exhibits mechanical properties that are at least equivalent to the mechanical properties of the polyetheretherketone (PEEK) connecting element. In another form, the center core has a non-circular cross-sectional shape and the first material is defined by a reinforcing material randomly dispersed throughout a polymer, and the outer portion includes a circular, outer cross-sectional shape. However, other embodiments, forms and applications are also envisioned.2011-05-05
20110106163Interlaminar Stabilizing System - A spinal stabilization system includes a first engagement member and a support structure. The first engagement member is adapted to be disposed between a first vertebra and a second vertebra. The engagement member generally includes a seating surface for accommodating at least a portion of a laminar region of the first vertebra. The support structure engages a portion of the second vertebra. The structural cooperation of the first engagement member and the support structure is such that the engagement member restricts reduction of the intervertebral spacing between the first and second vertebrae.2011-05-05
20110106164APPARATUS FOR IMPLEMENTING A SPINAL FIXATION SYSTEM WITH SUPPLEMENTAL FIXATION - An apparatus for implementing a spinal fixation system with supplemental fixation includes a spinal fixation rod assembly and at least one supplemental fixation device. The spinal fixation rod assembly is adapted to provide primary fixation at a plurality of first fixation points by being secured to a plurality of first vertebral components except not into one of the first vertebral components of the plurality that is in a weakened structural condition and located between other of the first vertebral components of the plurality. The supplemental fixation device is adapted to provide supplemental fixation for the assembly at a second fixation point by being secured to a second vertebral component located adjacent to and offset from the one first vertebral component in the weakened structural condition and also to interconnect with the assembly to provide anchorage and thus additional fixation supplemental to the primary fixation.2011-05-05
20110106165DEVICES AND METHODS FOR DYNAMIC SPINAL STABILIZATION AND CORRECTION OF SPINAL DEFORMITIES - An apparatus for attachment to a vertebral body for correcting spinal deformities. The apparatus has a plate member having an upper surface and a lower surface. The upper surface having at least one receiving member defining a channel for receiving a flexible connection member. The at least one receiving member having a proximal portion and a distal portion. The proximal and distal portions interfacing along a frangible connection such that the at least one receiving member extends axially from the upper surface a first distance when the frangible connection is unbroken and the at least one receiving member extends axially from the upper surface a second distance when the frangible connection is broken. The second distance is less than the first distance.2011-05-05
20110106166REVISION CONNECTOR FOR SPINAL CONSTRUCTS - A revision connector is configured to couple a new spine fixation rod to a previously implanted spine fixation rod that is secured to a plurality of vertebrae. The new spine fixation rod can be implanted and secured to vertebrae that are caudal and/or cranial with respect to the previously secured vertebrae.2011-05-05
20110106167ADJUSTABLE SPINAL STABILIZATION SYSTEM - An adjustable spinal stabilization system having a flexible connection unit for non-rigid stabilization of the spinal column. In one embodiment, the spinal stabilization system includes a flexible connection unit having a tether running through a hollow portion of the flexible connection unit, wherein the tether limits bending of the flexible connection unit. In a further embodiment the tether is pre-tensioned. In a further embodiment, the tension upon or compression of the tether is adjustable.2011-05-05
20110106168Laminoplasty Rod System - A laminoplasty rod and rod system that allows for variable angulation, translation (distraction and/or compression) and rotation of a spinal lamina bone portion associated with a laminoplasty, prior to fixation thereof. The laminoplasty rod is configured for use with a polyaxial spinal rod bone screw assembly that is adapted to be anchored to the vertebra associated with the laminoplasty, and is attachable to the spinal lamina bone portion. The laminoplasty rod system provides positional attachment of the laminoplasty rod to the spinal components associated with the laminoplasty and fixation thereof in various orientations. The laminoplasty rod system is characterized by a configured laminoplasty rod that fits into or onto the head of a polyaxial spinal rod bone screw assembly. A bone screw boss, defining a bone screw attachment configuration, is formed at one end of the laminoplasty rod. Preferably, but not necessarily, the bone screw boss is situated at an angled end of the rod having a pre-defined bend that provides for greater variation in rod orientation.2011-05-05
20110106169Bone Plate Holder - An instrument for holding a bone plate may include a first arm, a second arm connected to and adjustable relative to the first arm, a first connection tip at the distal end of the first arm configured to connect to the first side wall of the bone plate, and a second connection tip at the distal end of the second arm configured to connect to the second side wall of the bone plate. A stabilizing member is connected to the first connection tip. The stabilizing member is distally spaced apart from the first connection tip to form an opening for receiving a portion of bone between the first connection tip and the stabilizing member.2011-05-05
20110106170TACK FOR SPINE FIXATION - A tack for insertion into facets joints of the human spine includes one or more bioactive materials. The tack is preferably pushed/impacted axially into a hole in the facets, rather than rotated or screwed into the hole/facets. For example, the bioactive material may be outer sidewall(s) made of porous material that receives and/or encourages bone growth into its pores. Or, for example, the bioactive material may be osteobiologic material, demineralized bone matrix (DBM), sponge holding bone morphogenic protein (BMP), allograft bone, or other bioactive material inside an interior space of the tack. Apertures may be provided in the outer wall of a hollow tack to allow bone growth into the interior space of the tack. The tack may have a longitudinal passage, so that the tack may be installed on and slid along a guide-wire in percutaneous surgery that is guided by intraoperative imaging navigation. Preferably, the tack is not threaded, and is installed with little, and preferably no, rotation of the tack on its longitudinal axis.2011-05-05
20110106171SCREW IMPLANT AND SYSTEM AND METHOD FOR LOCKING A SCREW IN AN IMPLANT PLATE - A plate system and method comprising a plate and a screw having an integral resilient lock. The screw comprises a head that has a portion that is adapted to be compressible as it is screwed into bone using a tool. After the screw head is received in the plate and the tool is removed therefrom, the screw head decompresses or expands into a locking or receiving area, thereby locking the screw in the plate. The plate is adapted to have at least one or a plurality of detents or lips for cooperating with at least a portion of the screw head to retain the screw in the plate and prevent it from withdrawing therefrom.2011-05-05
20110106172SEMI-CONSTRAINED BONE SCREW - A bone screw for attaching a bone plate to bone includes a shank defining a lumen extending at least partially therethrough from a proximal end thereof, a head defining a lumen therethrough, and a rod member. The rod member is configured for insertion through the lumen of the head and into the lumen of the shank. The rod member is fixedly engageable with the shank and moveably coupled to the head such that both the rod member and the shank are moveable with respect to the head.2011-05-05
20110106173Anchor Assembly With Directionally Controlled Saddle Adjustment And Transversely Adjustable Receiver - A bone anchor assembly includes a receiver extending along a central longitudinal axis between a proximal end and an opposite distal end and a bone anchor extending from the receiver. The receiver includes a distal portion defining a receptacle opening at the distal end and a pair of arms extending from the distal portion along the central longitudinal axis on opposite sides of a passage. The receiver includes a saddle that is adjustable in the receiver in one plane to accommodate the angle of placement of the connecting element through the receiver. The receiver is adjustable in another plane that is transverse to the adjustment plane of the saddle to better position the receiver to receive the connecting element. The adjustable saddle and receiver reduce the bending or contouring of the connecting element that may be required to position the connecting element in the receiver.2011-05-05
20110106174Direct Control Spinal Implant - A bone anchor assembly is provided, which may be used in cervical, thoracic, lumbar or sacral areas of the spine or other orthopedic locations. The anchor assembly includes a bone anchor, a receiver mounted to the bone anchor, a saddle within the receiver, a spacer within the receiver, and an engaging member. The receiver extends along a central longitudinal axis proximally away from the bone anchor. A rod or other elongated connecting element is received in a passage of the receiver in contact with the saddle, and the engaging member engages the connecting element against the saddle, which engages the saddle against the spacer, which in turn engages the proximal head of the bone anchor in the receiver. The orientation of the saddle in the receiver is adjustable to correspond to the orientation of the connecting element relative to the central longitudinal axis of the receiver.2011-05-05
20110106175Bone Engaging Implant With Adjustment Saddle - A bone anchor assembly is provided, which may be used in cervical, thoracic, lumbar or sacral areas of the spine or other orthopedic locations. The anchor assembly includes a bone anchor, a receiver mounted to the bone anchor, a saddle within the receiver, and an engaging member. The receiver extends along a central longitudinal axis proximally away from the bone anchor. A rod or other elongated connecting element is received in a passage of the receiver in contact with the saddle, and the engaging member engages the connecting element against the saddle, which engages the saddle against the proximal head of the bone anchor in the receiver. The orientation of the saddle in the receiver is adjustable to correspond to the orientation of the connecting element relative to the central longitudinal axis of the receiver.2011-05-05
20110106176Polyaxial bone screw with multi-part shank retainer and pressure insert - A polyaxial bone screw assembly includes a threaded shank body having an upper portion, a receiver, a compression insert and an articulation structure made from at least two discrete pieces. The shank upper portion cooperates with the compression insert to place the retainer in frictional engagement with the receiver. The geometry of the retainer structure pieces corresponds and cooperates with the external geometry of the shank upper portion to frictionally envelope the retainer structure between the capture structure and an internal surface defining a cavity of the receiver.2011-05-05
20110106177ANCHOR FOR USE WITH ORTHOPEDIC SCREW - The invention provides devices and methods for stronger and more stable spinal and other orthopedic implant fixation through the use of an anchor for an orthopedic screw e.g, a pedicle screw. The anchor includes a relatively rigid proximal flange and a distal flexible portion that has an inner surface engageable by the screw shank as it is installed in a patient. For use, the distal portion of the anchor is located in a tract of the patient and the screw then installed through the anchor in the tract. During installation, outwardly-directed radial pressure of the screw shank upon inner surfaces of the flexible distal portion of the anchor can cause enhanced engagement of the bones or body structures by the anchor. The anchor flange can include teeth for engaging bones or other body structures, so as to provide improved support for the orthopedic installation.2011-05-05
20110106178PEDICLE SCREW HEAD EXTENDER - The present invention relates to pedicle screw spinal rod connectors and more specifically, a pedicle screw head extender for use with a pedicle screw to ease connection to a spinal rod. The pedicle screw head extenders provided herein can be used with either fixed head pedicle screws or multi-axial head pedicle screws. The pedicle screw head extenders can either be threaded to or snapped into place within the various pedicle screws. It may also be possible to use the present invention with other types of spinal screws that may be connected to spinal rods without the screw actually being implanted through the pedicle of the spine.2011-05-05
20110106179Set Screw Having Variable Pitch Thread for Use With Spinal Implant Systems - An improved set screw for use with spinal implants to attach an elongated member to a bone. The set screw has a body with a lower portion. An external thread is on the lower portion wherein at least a portion of the external thread has a variable pitch. The set screw will engage a receiver member by a predetermined longitudinal distance before encountering the variable pitch of the external thread on the set screw. A preselected torque value for seating the set screw is achieved at this predetermined longitudinal distance of thread engagement by the set screw into the receiver member. The variable pitch provides consistent clamping force even when excessive torque is applied to the set screw. An upper portion can be connected to the lower portion of the set screw through a frangible portion. The preselected torque value for seating the set screw is selected at a value less than the break-off or separation torque required to cause the frangible portion to separate the upper portion from the lower portion of the set screw.2011-05-05
20110106180Implants With Adjustable Saddles - A bone anchor assembly is provided, which may be used in cervical, thoracic, lumbar or sacral areas of the spine or other orthopedic locations. The anchor assembly includes a bone engaging portion, a receiver, a saddle within a channel defined by the receiver, and an engaging member. The receiver extends along a central longitudinal axis and is fixed to the bone engaging portion. A rod or other elongated connecting element is received in a channel of the receiver in contact with the saddle, and the engaging member engages the connecting element against the saddle. The orientation of the saddle in the receiver is adjustable to correspond to the orientation of the connecting element relative to the central longitudinal axis at any one of a plurality of angles of the connecting element through the receiver while the receiver and bone engaging portion remain fixed relative to one another.2011-05-05
20110106181ADJUSTABLE SADDLE FOR A BONE ANCHOR - A bone anchor is provided, which may be used in cervical, thoracic, lumbar or sacral areas of the spine or other orthopedic locations. The anchor includes an anchoring portion, a receiving portion, and an internal saddle that is rotatable with respect to the receiving portion at least to a degree. The anchoring portion is attachable to a bone. A rod or other elongated support member is received in the receiving portion in contact with the saddle. The rod and saddle may be rotated for variability substantially in a plane, and an engaging member is engaged to the receiving portion to lock the rod within the receiving portion.2011-05-05
20110106182DEVICE FOR OSTEOSYNTHESIS AND FOR IMMOBILIZATION AND STABILISATION OF TUBULAR BONES - shows an inventive implant 2011-05-05
20110106183Plate Holding Bone Forceps and Method of Use - A device for the positioning of a bone plate against a bone comprises first and second arms pivotally connected at a first joint, distal ends of the first and second arms defining a gripping surface for gripping the bone therebetween, proximal portions of the first and second arms extending in a first plane. An extension member couples to the first and second arms at the first joint and includes a first section extending distally from the first joint parallel to the first plane and a second section extending distally from the first section angled relative to the first section so that when the first and second arms are in a desired configuration gripping the bone, the second section extends parallel to the bone. A compression mechanism couples to the second section and includes a compression member and a coupling member being movable toward and away from the second section.2011-05-05
20110106184ANTERIOR INFLATION BALLOON - An inflatable bone tamp for performing a minimally invasive surgical procedure includes an inflatable structure that exhibits an outwardly tapering expansion profile. The outward taper can beneficially allow the inflatable bone tamp to exert greater targeted force in difficult environments. For example, in a vertebra with a compression fracture, the outwardly tapering expansion profile of the inflatable bone tamp can result in greater lifting force being applied to the endplates of the vertebra, thereby increasing the likelihood of restoring the height lost due to the compression fracture.2011-05-05
20110106185APPARATUS AND METHOD FOR APPLYING SUSTAINED TENSION ON A TETHER - Apparatus for applying sustained tension on tether in treatment site includes a positioning mechanism, gripping mechanism and pressurized fluid actuated mechanism. The positioning mechanism is operable to position the pressurized fluid actuated mechanism at a fixed distance relative to treatment site, and to engage a target at treatment site and secure the tether proximate to the target. The gripping mechanism is operable to selectively grip the tether and maintain tether when tether is held in tension. The pressurized fluid actuated mechanism is selectively operable to apply desired pulling force on gripping mechanism directed away from treatment site so as to transmit and apply in a sustained manner the desired pulling force on the tether independently from the tether displacement and place it under desired level of tension while the tether is being secured.2011-05-05
20110106186BONE FRAGMENT EXTRACTION - Methods and structures for removing a bone fragment from a body of a patent. A method can include advancing a distal portion of an orthopedic extraction device into a bone fragment disposed in a bone mass in the body of the patient, and actuating one or more deployable members of the distal portion of the device positioned in the bone fragment so as to engage the bone fragment with the device. With engagement between the device and bone fragment, a force or torque to the device so as to remove the bone fragment from the bone mass of the patient.2011-05-05
20110106187Instruments and methods for stabilization of bony structures - The present invention relates to methods and instruments for placing a brace or connecting element into an animal subject for engagement with anchors secured in the animal subject. The installation instrument includes anchor extensions coupled to the anchors. The instrument is movable with respect to the anchors to position the connecting element in a position more proximate the anchors.2011-05-05
20110106188IMPLANT ASSEMBLY - An implantable device is provided. The device is constructed from an open body containing electronic components, a heat-sensitive component, and a sealing component. The device is formed in a moisture controlled environment, such that the heat-sensitive component is attached to the open enclosure after the enclosure has been heated. The sealing component is subsequently affixed to the open enclosure to form a sealed enclosure.2011-05-05
20110106189IMPLANTABLE MEDICAL DEVICES INCLUDING ELONGATED CONDUCTOR BODIES THAT FACILITATE DEVICE AND LEAD CONFIGURATION VARIANTS - Implantable medical devices include elongated conductor bodies and related features including an attachment to the medical device at one end and a connector that receives a medical lead at the other end. The connector may have various features such as a modular design whereby the connector is constructed from a series of stacked contact modules. Other features of the connector include electrical contacts that are relatively thin conductors or the order of 0.040 inches or less and that may include radial protrusions to establish contact with the electrical connectors of the lead. Furthermore, electrical contacts may be mounted within the connector in a floating manner so that radial movement of the electrical contact may occur during lead insertion. Additional features include a feedthrough where conductors exposed beyond a housing of the implantable medical device make direct electrical connection to conductors present within the elongated body.2011-05-05
20110106190Defibrillator Having a Secure Discharging Circuit Comprising an H-Bridge - The invention relates to a cardiac defibrillator used to treat a patient in cardio-circulatory arrest by a shock from a dosed biphasic discharge from a capacitor through an H-bridge comprising a high-voltage switch A, B, C or D in each of the limbs thereof. Said cardiac defibrillator is characterised in that each opposing polarity phase of the biphasic shock is controlled in two stages in such a way that, for each pair of switches associated with a phase, the first switch is switched on and remains on during the entire phase, while the second switch switches off in a staggered manner in relation to the first switch for a controlled amount of time in order to pass the current through the patient during said phase, the same process being carried out for the second phase with the other pair of switches. The invention is especially suitable for manufacturers of defibrillation appliances.2011-05-05
20110106191IMPLANTABLE MEDICAL DEVICE NOISE MODE - Techniques for activating an alternative operating mode in an implantable medical device based on a determination that the device is within a relatively high noise environment or otherwise exposed to relatively high noise. The implantable medical device can automatically detect its presence in a high noise environment and automatically revert to the alternative operating mode, the device may be manually switched to alternative operating mode, or a hybrid manual/automatic approach may be used to switch the device to alternative operating mode.2011-05-05
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