01st week of 2011 patent applcation highlights part 43 |
Patent application number | Title | Published |
20110004212 | INTRAMEDULLARY MEDICAL DEVICE AND METHODS OF USE AND MANUFACTURE - Intramedullary medical devices (e.g., intramedullary nails) and methods for their use and manufacture are described herein. The intramedullary medical devices described herein may provide sustained compressive forces across a bone fusion site despite bone resorption processes. Through various embodiments, the intramedullary medical devices described herein may provide non-linear force curves relative to displacement. Intramedullary medical devices are described with multiple elements made of different materials. Examples of intramedullary medical devices are described with shape memory alloys. | 2011-01-06 |
20110004213 | SYSTEMS AND METHODS FOR INTERNAL BONE FIXATION - Internal bone fixation devices and methods for using the devices for repairing a weakened or fractured bone are disclosed herein. A device for use in repairing a fractured bone includes a delivery catheter having an elongated shaft with a proximal end, a distal end, and a longitudinal axis therebetween, wherein the delivery catheter has an inner void for passage of at least one reinforcing material and an inner lumen for passage of a light source; a conformable member releasably engaging the distal end of the delivery catheter, wherein the conformable member moves from a deflated state to an inflated state when the at least one reinforcing material is delivered to the conformable member; and an adapter releasably engaging the proximal end of the delivery catheter for receiving the light source and the at least one reinforcing material. | 2011-01-06 |
20110004214 | ORTHOPEDIC SURGICAL DEVICE - An osteotome may include a handle; a shaft coupled to the handle; a cutting member coupled to the shaft, wherein the cutting member comprises a first cutting surface positioned perpendicular to a second cutting surface, and wherein said first and second cutting surfaces extend downward relative to the shaft; and a stop means configured to control the depth of cut by the cutting member. | 2011-01-06 |
20110004215 | LABRUM RETRACTING BURR - A rotary abrader allowing for improved visibility during surgery and improved aspiration of waste material. This is accomplished by providing a hood or sheath formed of a clear material and available in various shapes and sizes. The clear hood or sheath is also provided with a flattened, angled portion at a tip of the hood, to assist with retraction of the labral tissue while burring the glenoid rim. Slots are provided on the cannulated tube to provide aspiration of waste material and used to attach the hood to the cannulated tube. | 2011-01-06 |
20110004216 | TIBIAL RASP - Methods and apparatus for arthroscopically-assisted preparation of the tibia to accept an unicompartmental implant that includes the step of removing bone from the tibial plateau to correct depth, diameter and proper angle by employing a tibial rasp comprising a cutter with a plurality of teeth on the bottom surface and a side surface (for example, the front side). The tibial rasp may be used in conjunction with an additional starter rasp that can cut only in one direction (for example, cutting to establish only the depth of the tunnel or socket). | 2011-01-06 |
20110004217 | Apparatus and Method for Injecting Fluent Material at a Distracted Tissue Site - A system and method is provided for distracting opposite surfaces from the interior of a bone, such as a vertebral body. A working channel cannula provides a working channel through which an inserter and an injection cannula can simultaneously pass. The inserter transports a plurality of wafers into the interior of the bone to form a load-bearing stack bearing against the opposite surfaces. The injection cannula is used to inject a fluent material into and/or around the stack. In certain embodiments, the fluent material is a load-bearing or hardenable material, such as bone cement. In other embodiments, the fluent material can be a BMP, HAP, or other osteo-inductive, osteo-conductive, or pharmaceutical compositions. A syringe containing the fluent material is engaged to the injection cannula and is operable to inject the fluent material into the vertebral body under controlled pressure. | 2011-01-06 |
20110004218 | Process for the preparation of NACRE mechano-structured by mechanosynthesis, mechano-structured NACRE thus obtained and uses thereof - The present invention relates to a method for the preparation of mechano-structured nacre by mechanosynthesis of micrometric nacre powder, characterized in that the temperature of the nacre is kept below 40° C. It also relates to the mechano-structured nacre and to uses thereof, in particular on implants and bone substitute pieces on which the mechano-structured nacre is deposited. | 2011-01-06 |
20110004219 | Calcium Phosphate Cements Comprising Autologous Bone - Aspects of the invention include methods for producing flowable compositions, e.g. pastes, that set into calcium phosphate containing products, where the products include autologous bone. Aspects of the invention further include compositions produced by the methods, as well as kits for preparing the same. The subject methods and compositions produced thereby find use in a variety of applications, including hard tissue repair applications. | 2011-01-06 |
20110004220 | CURABLE MATERIAL DELIVERY DEVICE WITH A ROTATABLE SUPPLY SECTION - An apparatus and method for introducing material into an injection site of a patient is disclosed. The device includes a cannula and a carrier. The cannula is inserted into an injection site of a patient. The carrier is connected to an injector containing a volume of material. Material may be pre-loaded into the carrier so that the material is delivered to a distal end of the carrier from the injector and the carrier is thus pre-loaded with material. A portion of the distal end of the pre-loaded carrier is inserted into the cannula and material is delivered to an injection site. The supply section can be rotatable with respect to the longitudinal axis of the inner section. | 2011-01-06 |
20110004221 | METHODS AND APPARATUS FOR DEPLOYING SHEET-LIKE MATERIALS - Implant delivery systems for delivering sheet-like implants include a delivery shaft, an implant expander, a sheath, and a sheet-like implant. In some embodiments, the delivery shaft has a proximal end and a distal end. The implant expander is mounted to the distal end of the delivery shaft. The implant expander includes a central portion and a plurality of leg portions radiating from the central portion. The implant expander is evertable between an unstressed configuration in which a distal surface of the implant expander defines a concave surface, and a first compact configuration in which the distal surface of the implant expander defines a convex surface. The implant expander has a first lateral extent when the implant expander is free to assume the unstressed configuration. The sheath defines a lumen having a lumen diameter. At least a portion of the delivery shaft is slidably disposed in the lumen. The lumen diameter is smaller than the first lateral extent of the implant expander so that the sheath holds the implant expander in the first compact configuration when slidably disposed therein. The sheet-like implant overlays at least a portion of the distal surface of the implant expander with portions of the sheet-like implant extending between the leg portions of the implant expander and the sheath. Methods of treating a rotator cuff of a shoulder are also disclosed. | 2011-01-06 |
20110004222 | Tool for Use with a Bone Anchor, in Particular for Spinal Surgery - A tool is provided for use with a bone anchor, wherein the bone anchor has an anchoring section and a receiving portion for receiving a rod to be connected to the anchoring section and a locking element, the tool comprising a tip portion for engaging the locking element; a mechanism to apply torque to the tip portion comprising a drive shaft and a driven shaft coupled by a gear unit, where the drive shaft has a different axis than the driven shaft, and where the driven shaft comprises an engagement portion configured to connect the driven shaft to the gear unit; and a counter-holding portion for engaging the receiving part, wherein the counter-holding portion is rotatable with respect to the tip portion. | 2011-01-06 |
20110004223 | VALVES AND HUBS FOR TUBULAR DEVICES AND METHODS FOR MAKING AND USING THEM - A hub for a sheath, catheter, or other tubular device includes a first hub portion including a first hub lumen sized for receiving a medical device therethrough, and a second hub portion including a second hub lumen, the second hub portion coupled to the first hub portion such that the first and second hub lumens are aligned with one another and the first and second hub portions are spaced apart from one another to define a gap. A valve is secured within the gap between the first and second hub portions that includes a valve passage therethrough, e.g., for accommodating receiving a medical device through the first and second hub lumens into the tubular device, while providing a substantially fluid tight seal. For example, the valve passage may include a bore extending partially from a first end of the valve towards a second end of the valve, and a slit that extends from the end of the bore to the second end of the valve. | 2011-01-06 |
20110004224 | TRACKING CAS SYSTEM - A computer-assisted surgery system for tracking an object during surgery comprises a first tracker device and a second tracker device secured to different parts of the object. The first and the second tracker device are secured to the object separately in such a way that a geometrical pattern is defined with trackable elements from the first tracker device and from the second tracker device. A tracking system has a sensor unit tracking the trackable members. A calibration unit defines a geometrical pattern from the trackable members. A pattern identifier identifies the geometrical pattern. A position and orientation calculator calculates a position and orientation of the geometrical pattern The tracking system calculates position and orientation of the object as a function of the position and orientation of the geometrical pattern and of object/geometrical pattern relation data gathered during surgery. | 2011-01-06 |
20110004225 | SURGICAL INSTRUMENT AND COUPLING STRUCTURE FOR SURGICAL ROBOT - Disclosed are a surgical instrument and a coupling structure for a surgical robot. The surgical instrument, which may be mounted on a surgical robot for operation, and which may perform a maneuver required for surgery by moving and rotating an effector joined to one end of the surgical instrument, may include: a first driving component that rotates about a first axis, a second driving component joined to the first driving component that rotates the first driving component about a second axis which intersects the first axis, a third driving component joined to the second driving component that rotates the second driving component about a third axis which intersects the second axis, a shaft joined to the third driving component that extends in one direction and has the effector joined to one end, and a housing that holds the first driving component, the second driving component, and the third driving component. As the driving components for moving the effector can be provided in a systematically connected form, instead of having each of the driving components arranged independently, the size of the surgical instrument may be reduced. Also, by forming the driving components as a 3-dimensional structure instead of using 2-dimensional pulleys, the transfer of forces required for the complex movements of the effector can be implemented simultaneously. Embodiments of the present invention can also readily be applied to a snake type surgical instrument. | 2011-01-06 |
20110004226 | AXIAL NEEDLE AND SUTURE DELIVERY DEVICE AND METHOD - A needle delivery device that has particular application for providing needles for minimally invasive spinal surgical procedures. The device includes an elongated pincher having opposing rails that is slidable within a channel defined in an extended base portion. Widened end portions of the rails hold the needle and push it out of an end of the device where it is released. The pincher is then retracted to a location where the end portions can pick up a next needle to be delivered. | 2011-01-06 |
20110004227 | FIXATION DEVICES FOR VARIATION IN ENGAGEMENT OF TISSUE - Devices, systems and methods are provided for tissue approximation and repair at treatment sites, particularly in those procedures requiring minimally-invasive or endovascular access to remote tissue locations. Fixation devices are provided to fix tissue in approximation with the use of distal elements. In some embodiments, the fixation devices have at least two distal elements and an actuatable feature wherein actuation of the feature varies a dimension of the at least two distal elements. In other embodiments, the fixation devices have at least two pairs of distal elements wherein the pairs of distal elements are moveable to engage tissue between opposed pairs of distal elements. Systems are also provided having fixation devices and accessories. | 2011-01-06 |
20110004228 | Systems and Methods for Treating Obesity and Type 2 Diabetes - The present invention provides systems and methods for treating and/or controlling obesity and type II diabetes. In one aspect of the invention, a device for treating obesity includes a flow restrictor and an anchor coupled to the flow restrictor. The flow restrictor is movable between a first or collapsed configuration sized and shaped for endoscopic advancement through the patient's esophagus and into a distal region of the stomach and a second or operative configuration sized and shaped for inhibiting a flow of chyme from the stomach to the pyloric sphincter. It is believed that this will cause the prolongation of satiety, and result in fewer meals being eaten and/or smaller meals being ingested. The anchor is movable between a first or collapsed configuration sized and shaped for advancement through the esophagus, stomach and pyloric sphincter and into the proximal region of the duodenum and a second or operative configuration sized and shaped to inhibit proximal movement of the anchor through the pyloric sphincter. | 2011-01-06 |
20110004229 | Systems and Methods for Treating Obesity and Type 2 Diabetes - The present invention provides systems and methods for treating and controlling obesity and/or type II diabetes. In one aspect of the invention, a bypass device includes gastric and duodenal anchors coupled to each other and positioned on either side of the pylorus and a hollow sleeve designed to extend from the pylorus through at least a proximal portion of a patient's small intestine. The gastric and duodenal anchors are movable between collapsed configurations for advancement through the esophagus and an expanded configuration for inhibiting movement of the anchors through the pyloric sphincter. Thus, the bypass device can be placed and removed endoscopically through the patient's esophagus in a minimally invasive outpatient procedure and it is “self-anchoring” and does not require invasive tissue fixation within the patient's GI tract, thereby reducing collateral tissue damage and minimizing its impact on the digestive process. | 2011-01-06 |
20110004230 | Atraumatic Gastrointestinal Anchor - The present invention relates to methods and articles for anchoring within a natural bodily lumen. An anchor is adapted to provide differing radially-outward forces along its length, a securing force and a transitional force. Production of these forces can be controlled by varying a physical property of the anchor, such as its stiffness, thickness, or shape. For example, the stiffness of an elongated anchor can be varied from a relatively soft value at its proximal and distal ends to a relatively stiff value at its center by varying the diameter of wire forming the anchor, thereby tailoring it to an intended application. Such force tailoring can be combined with external barbs and used to reliably anchor other instruments, such as feeding tubes and intestinal sleeves. | 2011-01-06 |
20110004231 | Percutaneous Gastroplasty - Disclosed are methods and apparatus for implantation into the walls of an organ such as the stomach. Deformable or inflatable anchors with a connector between are used to pull the walls of the organ together, or to implant devices in the wall of the organ. Also disclosed are surgical instruments useful in practicing the disclosed methods. | 2011-01-06 |
20110004232 | SURGICAL DEVICE USING WATER JET AND METHOD FOR OPERATING SAID DEVICE - A water jet surgical device comprises a fluid feed device, which is controllable by control signals from a control device, for delivering a fluid into a connecting line of a surgical instrument with an outlet nozzle. The fluid feed device includes at least one measuring device, which is configured such that following the connection of the surgical instrument to the fluid feed device, the measuring device generates measuring signals to represent a quantity of fluid delivered. The quantity of fluid delivered may be displayed on a display or recorded in a recording unit. This enables improved monitoring of surgical operations. | 2011-01-06 |
20110004233 | Hand Activated Ultrasonic Instrument - An ultrasonic surgical clamp coagulator apparatus is configured to effect cutting, coagulation, and clamping of tissue by cooperation of a clamping mechanism of the apparatus with an associated ultrasonic end-effector. The handle of the apparatus is configured to permit hand activation for cutting, coagulation, and clamping of tissue during surgical procedures. In order to promote convenient and efficient use of the apparatus, the fingertip controls are provided directly into the disposal shears handle in a position that allows surgeons to activate the device without repositioning their hand. The two buttons provide independent control of the two power levels available from the generator, matching the two foot pedal configuration of the prior art. | 2011-01-06 |
20110004234 | Systems and Methods for Treatment of Obesity and Type 2 Diabetes - The present invention provides systems and methods for treating and controlling obesity and/or type II diabetes. In one aspect of the invention, an internal bypass device includes gastric and duodenal anchors coupled to each other and positioned on either side of the pylorus and a hollow sleeve designed to extend from the pylorus through at least a proximal portion of a patient's small intestine. The gastric and duodenal anchors are movable between collapsed configurations for advancement through the esophagus and an expanded configuration for inhibiting movement of the anchors through the pyloric sphincter. Thus, the bypass device can be placed and removed endoscopically through the patient's esophagus in a minimally invasive outpatient procedure and it is “self-anchoring” and does not require invasive tissue fixation within the patient's GI tract, thereby reducing collateral tissue damage and minimizing its impact on the digestive process. | 2011-01-06 |
20110004235 | TRANSAPICAL HEART PORT - This document relates to medical devices. For example, transapical heart ports, methods for making transapical heart ports, and methods for using transapical heart ports are provided. | 2011-01-06 |
20110004236 | Systems and Methods for Treating Obesity and Type 2 Diabetes - The present invention provides systems and methods for treating and controlling obesity and/or type II diabetes. In one aspect of the invention, a delivery system for deploying an implant to a target region in the GI tract of a patient comprises an enclosure and an introducer. The enclosure houses at least a portion of the implant and comprises a material designed to dissolve within the patient. The introducer is coupled to the enclosure and configured for advancing the enclosure (and the implant housed therein) through an esophagus and into a stomach of the patient. In a preferred embodiment, the enclosure comprises a biocompatible material that will dissolve in less than one hour, preferably less than 30 minutes, such as gelatin or the like. | 2011-01-06 |
20110004237 | MINIMAL SURFACE AREA CONTACT DEVICE FOR HOLDING PLAQUE TO BLOOD VESSEL WALL - A tack device for holding plaque against blood vessel walls in treating atherosclerotic occlusive disease is formed as a thin, annular band of durable, flexible material having a plurality of focal elevating elements on its outer annular periphery for holding loose plaque under a spring or other expansion force against a blood vessel wall. The focal elevating elements are designed to exert a holding force on a plaque position while minimizing the amount of material surface area in contact with the plaque or blood vessel wall and reducing the potential of friction with the intraluminal surface. This approach offers clinicians the ability to perform a minimally invasive post-angioplasty treatment and produce a stent-like result without using a stent. | 2011-01-06 |
20110004238 | INTRAVASCULAR DEVICE AND SYSTEM - A device for use in capturing or collecting debris found in blood vessels or other body lumens. The devices can be fabricated from a tube and include longitudinally and circumferentially extending members. The device can further embody structure that provides enhanced radial opening and angular resistance to collapse and structure for absorbing or modifying forces applied thereto by an operator. | 2011-01-06 |
20110004239 | ROLLED TIP RECOVERY CATHETER - A distal tip for use with a medical catheter. The tip includes a member having a wall which defines a lumen therewithin. The wall has a portion at a distal end thereof, the portion curving inwardly toward an axis of the lumen. The lumen is provided with a diameter adaptable to accommodate a device to be recovered therewithin. | 2011-01-06 |
20110004240 | VISIBLE LIGHT CURABLE ADHESIVE - An object of the present invention is to provide a water soluble bioadhesive that is curable by visible light irradiation. The present invention provides a visible light curable adhesive, which comprises a water soluble oxygen sensitizer that generates radicals under visible light irradiation and a water soluble polymer compound having a functional group that can be activated via singlet oxygen generated from the oxygen sensitizer under visible light irradiation. | 2011-01-06 |
20110004241 | ADHESIVE - Methods comprising: providing a migrate-sensitive substrate having a surface to be bonded; providing an adhesive formulation comprising an isocyanate-terminated polyurethane prepolymer containing one or more tertiary amino groups; and forming a migrate-free adhesive bond between the surface of the migrate-sensitive substrate and a second surface; as well as adhesive formulations comprising an isocyanate-terminated polyurethane prepolymer containing one or more tertiary amino groups; and wound closure systems comprising such an adhesive formulation. | 2011-01-06 |
20110004242 | KNOTLESS SUTURE FIXATION DEVICE AND METHOD - A knotless suture fixation device ( | 2011-01-06 |
20110004243 | SEGMENTED SUTURE ANCHOR - A segmented suture anchor for fixation of soft tissue to bone. The segmented suture anchor is formed of multiple body segments that allow the suture anchor to be inserted and passed through a curved instrument such as a curved cannulated guide. At least two of the multiple body segments are connected by a strand of material (for example, a flexible suture strand, a suture tape, nitinol strand, or high-strength suture). The strand of material may be attached to the anchor by a connecting region (for example, a bonded or knotted region). The strand of material may also form a closed loop or eyelet attached to the suture anchor, to allow additional suture strands to be loaded through the closed loop or eyelet and aid in the fixation of soft tissue. | 2011-01-06 |
20110004244 | Vented pacifier - The present invention is a pacifier having a non-collapsible aperture within the nipple lengthwise and a vertical aperture crosswise. The pacifier has a superiorly arched nipple upon a guard and opposite the nipple, a tab for grasping. The horizontal aperture extends from the tip of the nipple and through the guard. The horizontal aperture allows the passage of air into and out of the pacifier as an infant breathes and has a rib extending lengthwise that prevents collapse of the aperture. However, as infants salivate when suckling on a pacifier, the vertical aperture permits drainage of saliva, that enters the horizontal aperture, back into the mouth of an infant. The guard has a generally oval shape. Alternatively, the nipple deviates superiorly and close to the proximal end, has recesses for teeth or gums, and a hole in the tab for a strap or keeper. | 2011-01-06 |
20110004245 | Spine Fixation Device - A spine fixation device is provided. The spine fixation device includes a bone screw, a fixation carrier, and a first locking member. The fixation carrier is rotatably coupled to a fixation unit of the bone screw. The first locking member conjugates the fixation carrier and the bone screw together. A screw unit of the bone screw is implanted into a vertebra. As the fixation carrier is rotatably coupled to the bone screw, the bone screw remains fastened to the vertebra while the fixation carrier is rotated. Through rotational adjustment of the fixation carrier, U-shaped openings of the fixation carrier are adjustable in direction. Thus, the disposition angle of a rod disposed in the U-shaped openings is easily adjustable by rotating the fixation carrier. As a result, the rod can fit an angle of the spine while surgical complexity is reduced. | 2011-01-06 |
20110004246 | INTERNAL OSTEODISTRACTION DEVICE - The invention relates to an internal osteodistraction device, which includes two fixing points ( | 2011-01-06 |
20110004247 | FACET INTERFERENCE SCREW - A facet interference screw ( | 2011-01-06 |
20110004248 | SPINAL STABILIZATION SYSTEMS AND METHODS OF USE - Devices and methods are adapted to permit fixation and stabilization of the bony elements of the skeleton. The devices permit adjustment and maintenance of the spatial relationship between neighboring bones. The motion between adjacent skeletal segments may be maintained, limited or completely eliminated. | 2011-01-06 |
20110004249 | FLEXIBLE SPINAL FIXATION DEVICE AND ROD THEREOF - A flexible spinal fixation device and a rod thereof are provided. The flexible spinal fixation device includes at least two bone screws and a rod. The rod is fixedly coupled to the bone screws, and the bone screws are implanted into a patient's vertebrae. The rod has a flexible part and is thereby rendered flexible. After the flexible spinal fixation device is implanted into the patient's spine, the patient's spine can stoop as in a healthy condition. Moreover, vertebral stress around an injured vertebra and force between the bone screws and the rod can both be reduced. The flexible spinal fixation device also prevents premature vertebral aging and has an extended service life. | 2011-01-06 |
20110004250 | Apparatus for Occipital-Cervical Fixation Enabling Supplemental Occipital Bone Fixation - An apparatus for stabilization of a patient's head relative to the patient's neck joint includes an occi-cervical base member having a “C’-shaped central part and first and second attachment rods respectively connected to and extending transversely from free ends of the central part. An occiput attachment has a first end slideably engaged to the central part and a flat, straight second end that extends radially outwardly relative to the first end. First and second polyaxial screw heads are adapted to be implanted in first and second occipital condyles of a patient, respectively. The first and second polyaxial screw heads are adapted to engage first and second stabilizing rods, respectively, that are placed in-line with the cervical spine of a patient and to engage the first and second attachment rods, respectively. | 2011-01-06 |
20110004251 | SPINAL FIXATION SYSTEM - A spinal fixation system includes a pedicle screw having a longitudinal axis. A fixation element is configured to connect the pedicle screw to at least one additional pedicle screw. A coupling mechanism includes a pedicle screw securing device adapted to secure the coupling mechanism to the pedicle screw and a fixation element securing device configured to secure the coupling mechanism to the fixation element. A fastening mechanism is configured to fasten both the pedicle screw securing device and the fixation element securing device. The fastening mechanism is located along the longitudinal axis of the pedicle screw. | 2011-01-06 |
20110004252 | PLATE FOR THE TREATMENT OF BONE FRACTURES - A plate is provided for the treatment of bone fractures, the plate having a first surface and a second surface, the second surface being opposed to the first surface and being adapted to face a bone surface. At least one of the first and second surfaces defines at least one generally linearly shaped portion of a boundary of at least one cross section of the plate. | 2011-01-06 |
20110004253 | SPINAL FIXATION PLATE - Spinal fixation plates for maintaining adjacent vertebrae in and fixed position are provided. In an exemplary embodiment, the plate includes opposed superior and inferior portions that are angled in a direction anterior to an anterior face of a mid-portion of the plate. The plate also includes a curvature formed therein about a longitudinal axis in a sagittal plane thereof. In use, when the plate is attached to adjacent vertebrae, the angle of the superior and inferior portions and the curvature in the plate are effective to position one or more thru-bores formed in the superior and inferior portions at the anterior rims of the adjacent vertebrae. In another embodiment, a spinal fixation plate is provided that is adapted to engage and mate to a fusion cage or other vertebral implant disposed between adjacent vertebra. The present invention also provides spinal fixation kits or assemblies, and methods for implanting the same. | 2011-01-06 |
20110004254 | Magazine for receiving at least one bone screw and bone plate having such a magazine - To facilitate the insertion of bone screws into a bone plate, a magazine for receiving at least one bone screw is proposed, which comprises a device for releasably securing the magazine to a bone plate, a receiving chamber extending continuously from the upper side to the underside of the magazine, a bone screw being arranged in the receiving chamber in such a way that when the magazine is secured to the bone plate, the distal tip of the bone screw is directed at a screw-in opening in the bone plate, and the proximal end of the bone screw is accessible to a screwing-in tool from the upper side of the magazine, and a fixing device for releasably fixing the bone screw in the receiving chamber. The invention also relates to a bone plate having at least one such magazine releasably secured thereto. | 2011-01-06 |
20110004255 | BONE JOINING APPARATUS AND METHOD - Provided is a bone joining device suitable for joining a first bone piece to a second bone piece. Also provided is a method of joining a first bone piece with a second bone piece in a living mammal. The method comprises inserting the above bone joining device between the first bone piece and the second bone piece. | 2011-01-06 |
20110004256 | INSTRUMENTS FOR USE WITH A BONE ANCHOR WITH PLUG MEMBER - Instruments for use with a bone anchoring assembly having plug member are disclosed that allow introduction of the plug member and bone cement or other liquid or pasty material into the bone anchor. The bone anchor includes a shaft having a first end and a second end, a channel extending from the first end to the second end, and a plug member which is insertable into the channel and guidable through the channel for closing the channel at the second end. The bone anchor is suitable for minimally invasive surgery in such a way a guide wire can be guided through the bone anchor and after the bone anchor has been anchored in the bone the plug member is inserted to close the open end of the bone anchor. | 2011-01-06 |
20110004257 | Implant Structure - An implant structure is provided. The implant structure includes an implant body and a screw portion. The screw portion is coupled to a second surface of the implant body such that the implant structure can be implanted into an injured bone via the screw portion. Thus, the implant body partially replaces and thereby repairs the injured bone. Threads of the screw portion have at least a barb unit for preventing the implant structure from rotating in the loosening direction of the screw portion. The at least a barb unit also prevents the implant structure from loosening and displacement so that the service life of the implant structure can be extended. | 2011-01-06 |
20110004258 | Fixation Device for Delivery of Biologic Material Between Soft Tissue and Bone - A fixation device for delivery of biological material between soft tissue and bone. The fixation device includes an anchor having a first longitudinal bore and a first radial extending delivery bore and an insert having a second longitudinal bore and a second radial extending delivery bore. The first and second radial extending bores are aligned and positioned relative to a head of the anchor to deliver the biologic material between the soft tissue and the bone. | 2011-01-06 |
20110004259 | REFERENCE FRAME FIXATOR - A device for positioning a fiducial marker ( | 2011-01-06 |
20110004260 | ARTHROSCOPIC TIBIAL SIZER - An arthroscopic tibial sizer provided with a collapsible loop (for example, a nitinol loop) and a pin indicator located at about the center of the collapsible loop. The collapsible loop is formed of a flexible wire (for example, nitinol wire) and is designed to collapse so that it can be inserted through an arthroscopic portal and into the joint, and then to expand out to its original diameter once inside the joint space, for visual sizing. The collapsible loop may be provided in various diameters (i.e., 14, 17 or 20 mm, for example) to match various implant sizes. The pin indicator indicates the center of the loop and provides identification of the center of the tibial defect. | 2011-01-06 |
20110004261 | ELECTROMAGNETIC THERMAL THERAPY - A portable, non-invasive device for providing therapeutic treatment to a joint to promote healing of the joint includes a cuff positionable around the joint. The cuff includes an electromagnetic stimulator configured to provide an electromagnetic field within the joint and a single-use thermal exchange component configured to provide temperature-based therapy to the joint. | 2011-01-06 |
20110004262 | VAGAL STIMULATION DURING ATRIAL TACHYARRHYTHMIA TO FACILITATE CARDIAC RESYNCHRONIZATION THERAPY - The disclosure describes techniques for delivering vagal stimulation to decrease the ventricular rate response during an atrial tachyarrhythmia, such as atrial fibrillation. Decreasing the ventricular rate response during an atrial tachyarrhythmia may facilitate increased ventricular pacing for cardiac resynchronization therapy (CRT), and may also reduce the likelihood of inappropriately detecting a ventricular tachyarrhythmia during the atrial tachyarrhythmia. Furthermore, the vagal stimulation may augment vagal tone, which may facilitate long term left ventricular reverse remodeling and decrease atrial and ventricular arrhythmic burden in heart failure patients. An example system that delivers CRT comprises a processor that detects an atrial tachyarrhythmia in one or more atria of the heart, and monitors at least one of a ventricular rate or degree of ventricular pacing subsequent to the detected atrial arrhythmia. The processor controls a stimulation generator to deliver vagal stimulation based on the least one of a ventricular rate or degree of ventricular pacing. | 2011-01-06 |
20110004263 | DATA-DRIVEN PATTERN DETECTION OF IMPLANTABLE MEDICAL DEVICE DATA - Detecting patterns in sensed implantable medical device (IMD) data is described. One implementation involves an IMD that includes a data-driven pattern detection network embodied on the IMD to detect a pattern from sensed patient data. The IMD also includes one or more algorithms embodied on the IMD to utilize the pattern to effect patient therapy. | 2011-01-06 |
20110004264 | Systems and Methods for Ranking and Selection of Pacing Vectors - Approaches to rank potential left ventricular (LV) pacing vectors are described. Early elimination tests are performed to determine the viability of LV cathode electrodes. Some LV cathodes are eliminated from further testing based on the early elimination tests. LV cathodes identified as viable cathodes are tested further. Viable LV cathode electrodes are tested for hemodynamic efficacy. Cardiac capture and phrenic nerve activation thresholds are then measured for potential LV pacing vectors comprising a viable LV cathode electrode and an anode electrode. The potential LV pacing vectors are ranked based on one or more of the hemodynamic efficacy of the LV cathodes, the cardiac capture thresholds, and the phrenic nerve activation thresholds. | 2011-01-06 |
20110004265 | MEDICAL DEVICE PACKAGING SYSTEM - A system, comprising a sterilizable package; an implantable medical device placed inside the sterilizable package; and an electrical interface electrically coupled to the implantable medical device and extending from inside the sterilizable package to outside the sterilizable package. In various embodiments, the interface may include package contacts electrically coupled to electrode terminals on the implantable medical device, patient terminals and conductors extending between the package contacts and the patient terminals. | 2011-01-06 |
20110004266 | Method and Apparatus for Treatment of the Gastrointestinal Tract - A method and device for electrically stimulating one or more structures in the gastrointestinal tract as described. The one or more structures are preferably selected from the upper esophageal sphincter, the esophagus and gastric fundus. The method may involve the step of arranging a plurality of stimulating electrodes adjacent one or more structures which may further include the lower esophageal sphincter, the stomach, the pyloric sphincter, the small intestine, the colon and the vagus. The method and device may further include sensing electrodes to detect change in one or more physiological parameters in the gastrointestinal tract and modulate the stimulating electrodes in response to the change. The device comprises a pulse generator, a power source, a plurality of stimulating electrode set, one or more sensing electrodes and means for varying activity of the stimulating electrodes in response to change detected in the gastrointestinal tract. The method and device may be used to treat obesity and/or GERD. | 2011-01-06 |
20110004267 | DEVICES AND METHODS FOR BRAIN STIMULATION - A device for brain stimulation that includes a lead having a longitudinal surface; at least one stimulation electrode disposed along the longitudinal surface of the lead; and at least one recording electrode, separate from the at least one stimulation electrode, disposed along the longitudinal surface of the lead. | 2011-01-06 |
20110004268 | Responsive Electrical Stimulation for Movement Disorders - An implantable neurostimulator system for treating movement disorders includes a sensor, a detection subsystem capable of identifying episodes of a movement disorder by analyzing a signal received from the sensor, and a therapy subsystem capable of supplying therapeutic electrical stimulation to treat the movement disorder. The system treats movement disorders by detecting physiological conditions characteristic of an episode of symptoms of the movement disorder and selectively initiating therapy when such conditions are detected. | 2011-01-06 |
20110004269 | IMPLANTABLE PULSE GENERATOR FOR PROVIDING FUNCTIONAL AND/OR THERAPEUTIC STIMULATION OF MUSCLES AND/OR NERVES AND/OR CENTRAL NERVOUS SYSTEM TISSUE - Improved assemblies, systems, and methods provide an implantable pulse generator for prosthetic or therapeutic stimulation of muscles, nerves, or central nervous system tissue, or any combination. The implantable pulse generator is sized and configured to be implanted subcutaneously in a tissue region. The implantable pulse generator includes an electrically conductive laser welded titanium case. Control circuitry is located within the case, and includes a primary cell or rechargeable power source, a receive coil for receiving an RF magnetic field to recharge the rechargeable power source, and a microcontroller for control of the implantable pulse generator. Improved assemblies, systems, and methods also provide a stimulation system for prosthetic or therapeutic stimulation of muscles, nerves, or central nervous system tissue, or any combination. The stimulation system provides at least one electrically conductive surface, a lead connected to the electrically conductive surface, and an implantable pulse generator electrically connected to the lead. | 2011-01-06 |
20110004270 | METHODS AND APPARATUS FOR EFFECTUATING A LASTING CHANGE IN A NEURAL-FUNCTION OF A PATIENT - The following disclosure describes several methods and apparatus for intracranial electrical stimulation to treat or otherwise effectuate a change in neural-functions of a patient. Several embodiments of methods in accordance with the invention are directed toward enhancing or otherwise inducing a lasting change in neural activity to effectuate a particular neural-function. Such lasting change in neural activity is defined as “neuroplasticity.” The methods in accordance with the invention can be used to treat brain damage (e.g., stroke, trauma, etc.), brain disease (e.g., Alzheimer's, Pick's, Parkinson's, etc.), and/or brain disorders (e.g., epilepsy, depression, etc.). The methods in accordance with the invention can also be used to enhance neural-function of normal, healthy brains (e.g., learning, memory, etc.), or to control sensory functions (e.g., pain). Certain embodiments of methods in accordance with the invention electrically stimulate the brain at a stimulation site where neuroplasticity is occurring. The stimulation site may be different than the region in the brain where neural activity is typically present to perform the particular neural function according to the functional organization of the brain. In one embodiment in which neuroplasticity related to the neural-function occurs in the brain, the method can include identifying the location where such neuroplasticity is present. In an alternative embodiment in which neuroplasticity is not occurring in the brain, an alternative aspect is to induce neuroplasticity at a stimulation site where it is expected to occur. Several embodiments of these methods that are expected to produce a lasting effect on the intended neural activity at the stimulation site use electrical pulses that increase the resting membrane potential of neurons at the stimulation site to a subthreshold level. | 2011-01-06 |
20110004271 | VISUAL PROSTHESIS SYSTEM FOR DISPLAYING VIDEO IMAGE AND TEXT DATA - A visual prosthesis system comprises a retina implant at least partly located in the interior of a patient's eye. The retina implant comprises an array of micro-contacts adapted for contacting ganglia of the patient's retinal tissue. The visual prosthesis system further comprises a data processing unit with an additional interface for receiving an external signal from an external signal source, the data processing unit being adapted for converting the external signal into corresponding stimulation data for the retina implant, and a wireless transmission unit adapted for transmitting the stimulation data to the retina implant via wireless transmission. The retina implant is adapted for receiving the stimulation data and for stimulating the micro-contacts according to the stimulation data. | 2011-01-06 |
20110004272 | SCANNING LASER DEVICE AND METHODS OF USE - In one aspect, the invention provides vision prosthesis systems. Exemplary vision prosthesis systems of the invention comprise a light energy generator operably connected to a wearable head piece comprising a device for directing light energy produced by the light energy generator onto a mammalian retina, wherein the light energy generator is tuned to emit light energy of sufficient power to modulate neural activity in the retina. In another aspect, the invention provides methods for irradiating neurons in the retina of the mammalian eye by directing light energy produced by a light energy generator onto a mammalian retina. The methods of the invention may be used to directly modulate the activity of retinal neurons or to introduce molecules into retinal cells. | 2011-01-06 |
20110004273 | SOUND COMMAND TO STIMULATION CONVERTER - A method and system for stimulating a tissue-stimulating prosthesis is disclosed. The method and system comprise receiving a sound command, such a MIDI command, and converting the sound to a stimulation signal. The stimulation signal is then used to provide stimulation to a recipient so that the recipient may perceive sound in accordance with the received sound command. | 2011-01-06 |
20110004274 | Cochlear Implant Stimulation with Low Frequency Channel Privilege - A system and method for activating stimulation electrodes in cochlear implant electrode is described. A preprocessor filter bank processes an input acoustic audio signal to generate band pass signals that each represent an associated band of audio frequencies. An information extractor extracts stimulation signal information from the band pass signals based on assigning the band pass signals to corresponding electrode stimulation groups that each contain one or more stimulation electrodes, and generates a set of stimulation event signals for each electrode stimulation group that define electrode stimulation timings and amplitudes. A pulse selector selects a set of electrode stimulation signals from the stimulation event signals based on a pulse weighting function that uses channel-specific weighting factors favoring lower frequencies for activating the stimulation electrodes to stimulate neighboring audio nerve tissue. | 2011-01-06 |
20110004275 | External Device for an Implantable Medical System Having Accessible Contraindication Information - Disclosed is a remote controller for an implantable medical device having stored contraindication information, which includes information which a patient or clinician might wish to review when assessing the compatibility of a given therapeutic or diagnostic technique or activity with the patient's implant. The stored contraindication information is available through a display of the remote controller or via a wired, wireless, or portable drive connection with an external device. By storing contraindication information with the implant's remote controller, patient and clinician can more easily determine the safety of a particular therapeutic or diagnostic technique or physical activity with the patient's implant, perhaps without the need to contact the manufacturer's service representative. | 2011-01-06 |
20110004276 | METHOD AND APPARATUS TO DETECT TRANSPONDER TAGGED OBJECTS AND TO COMMUNICATE WITH MEDICAL TELEMETRY DEVICES, FOR EXAMPLE DURING MEDICAL PROCEDURES - The presence or absence of objects tagged with transponders may be determined in an environment in which medical procedures are performed via an interrogation and detection system which includes a controller and a plurality of antennas positioned along a patient support structure. The antennas may be positioned along an operating table, bed, mattress or pad, sheet, or may be positioned on a drape, or shade. Respective antennas may successively be activated to transmit interrogation signals. Multiple antennas may be monitored for responses from transponders to the interrogation signals. For example, all antennas other than the antenna that transmitted the most recent interrogation signal may be monitored. Antennas may be responsive to force, a signal indicative of such force being produced. A wireless physiological condition monitor may detect patient physiological conditions and wirelessly transmit signals indicative of such. | 2011-01-06 |
20110004277 | System and Method for Managing Locally-Initiated Medical Device Interrogation - A system and method for managing locally-initiated medical device interrogation is presented. An interface is provided over which to retrieve patient data recorded and transiently staged by a medical device monitoring physiological measures of a patient. The patient data is periodically retrieved by interfacing to and interrogating the medical device per a pre-defined schedule through the interface. Further retrieval of the patient data is permitted independent of the pre-defined schedule. The system stores remotely-specifiable criteria specified by a caregiver and controls patient-initiated patient data retrieval in accordance with the criteria. | 2011-01-06 |
20110004278 | External Charger for a Medical Implantable Device Using Field Sensing Coils to Improve Coupling - By incorporating magnetic field sensing coils in an external charger, it is possible to determine the position of an implantable device by sensing the reflected magnetic field from the implant. In one embodiment, two or more field sensing coils are arranged to sense the reflected magnetic field. By comparing the relative reflected magnetic field strengths of the sensing coils, the position of the implant relative to the external charger can be determined. Audio and/or visual feedback can then be communicated to the patient to allow the patient to improve the alignment of the charger. | 2011-01-06 |
20110004279 | Implantable medical device connector - Disclosed is an implantable medical device including a connector block that allows varied lead configurations to be used with a single connector block and implantable medical device assembly. The connector block is configured with one or more lead insertion lumens that are open at both ends, such that each end of the lead insertion lumen may receive a separate lead. The circuitry within the implantable medical device is configured to allow the delivery of electrical pulses from a pulse generator within the implantable medical device to two separate leads, or to a single lead (with a plug positioned within the opposite, open end of the insertion lumen), inserted within a single lead insertion lumen. | 2011-01-06 |
20110004280 | TREATMENT OF SKIN DISORDERS WITH UV LIGHT - Skin disorders such as, for example, atopic dermatitis, dyshidrosis, eczema, lichen planus, psoriasis, and vitiligo, are treated by applying high doses of ultraviolet light to diseased regions of a patients skin. The dosage employed exceeds 1 MED, an MED being determined for the particular patient being treated, and may range from about 1 MED to about 20 MED or higher. The ultraviolet light has a wavelength within the range of between about 295 nanometers to about 320 nanometers and preferably is between about 300 nanometers and about 310 nanometers. High doses of ultraviolet light are restricted to diseased tissue areas so as to avoid risk of detrimental side affects in healthy skin, which is more susceptible to damage from UV light. Cooling the skin prior to and/or while exposing the skin to the UV light can be used to minimize tissue damage resulting from exposure to the UV light. Higher doses of UV light can therefore be employed without injurious affects. | 2011-01-06 |
20110004281 | IMPLANTABLE ANCHOR WITH LOCKING CAM - There is disclosed various embodiments of an implantable anchor for anchoring a medical lead within a patient. The implantable anchor includes a body having at least one lumen for receiving a medical lead, a cam integrated with the body and rotatable to extend into the lumen for engaging the medical lead and inhibiting the movement of the lead with respect to the anchor. The cam may include a handle for facilitating the rotation of the cam. A needle could be connected to the handle to facilitate the securing of the anchor to a portion of the patient. | 2011-01-06 |
20110004282 | Drug Eluting Lead Systems - Medical electrical lead systems and related methods are described. The lead systems may be configured to be at least partially implanted in neural tissue of a subject, such as a brain of a subject. Some variations of the lead systems may comprise a lead body, an electrode connected to the lead body, and a bioactive agent. The electrode and/or lead body may comprise a substrate, and the bioactive agent may be supported by the substrate (e.g., by a substantial portion of the area of the substrate). Examples of bioactive agents that may be used in the lead system include bioactive agents that promote neural adhesion and living cells that have been biologically manipulated, engineered cells, and cells of a particular phenotype and/or adapted to induce a desired neural or glial response. Methods described herein may comprise contacting the substrate of a lead body and/or an electrode of a medical electrical lead system with at least one bioactive agent, where the lead body and the electrode are connected to each other. | 2011-01-06 |
20110004283 | SHIELDED THREE-TERMINAL FLAT-THROUGH EMI/ENERGY DISSIPATING FILTER - A shielded three-terminal flat-through EMI/energy dissipating filter includes an active electrode plate through which a circuit current passes between a first terminal and a second terminal, a first shield plate on a first side of the active electrode plate, and a second shield plate on a second side of the active electrode plate opposite the first shield plate. The first and second shield plates are conductively coupled to a grounded third terminal. In preferred embodiments, the active electrode plate and the shield plates are at least partially disposed with a hybrid flat-through substrate that may include a flex cable section, a rigid cable section, or both. | 2011-01-06 |
20110004284 | ELECTROMAGNETIC INTEREFERENCE IMMUNE PACING/DEFIBRILLATION LEAD - An electromagnetic interference immune defibrillator lead has a first electromagnetic insulating layer. A first layer is formed on the first electromagnetic insulating layer, the first layer having a plurality of first conductive rings composed of first conductive material, each first conductive ring being separated by first insulating material. A second electromagnetic insulating layer is formed on the first layer. A second layer is, formed on the second electromagnetic insulating layer, the second layer having a plurality of second conductive rings composed of second conductive material, each second conductive ring being separated by second insulating material. A third electromagnetic insulating layer is formed on the second layer. The second conductive rings of second conductive material are positioned such that a second conductive ring overlaps a portion of a first conductive ring and overlaps a portion of a second conductive ring, the second conductive ring being adjacent to the first conductive ring. The second electromagnetically insulating layer is composed of a self-healing dielectric material. | 2011-01-06 |
20110004285 | SYSTEM AND METHOD FOR CARDIAC LEAD - An implantable medical device (IMD) can include implantable pulse generator (IPG) devices, implantable cardioverter-defibrillators (ICD), cardiac resynchronization therapy defibrillator devices, neurostimulators or combinations thereof. In one example, the IMD can include a body assembly, which can provide at least one electrical signal corresponding to a therapy. The IMD can also include a cardiac lead assembly, which can have a proximal portion and a distal portion. The proximal portion of the cardiac lead assembly can be in communication with the body assembly to receive the therapy and the distal portion can be adapted to be coupled to an anatomical structure to transmit the at least one electrical signal to the anatomical structure. The proximal portion of the cardiac lead assembly can have a first stiffness and the distal portion can have a second stiffness. The first stiffness can be greater than the second stiffness. | 2011-01-06 |
20110004286 | SYSTEM AND METHOD FOR CARDIAC LEAD - An implantable medical device (IMD) can include implantable pulse generator (IPG) devices, implantable cardioverter-defibrillators (ICD), cardiac resynchronization therapy defibrillator devices, neurostimulators or combinations thereof. The IMD can also include a cardiac lead assembly in communication with the body assembly to transmit the at least one electrical signal to an anatomical structure. The cardiac lead assembly can include a first sleeve, which can have a distal end, a proximal end, and a surface therebetween. The surface can define a plurality of annular ribs along the distal end and can have a channel defined between each pair of adjacent ribs. An electrode can be coupled to the surface of the first sleeve adjacent to the distal end such that at least one channel is fillable with an adhesive to couple a second sleeve to the first sleeve. | 2011-01-06 |
20110004287 | Bifurcated Stent and Delivery System - Systems for delivering a bifurcated stent to a bifurcation site comprise catheters and/or bifurcated stents delivered therefrom. | 2011-01-06 |
20110004288 | INTRAVASCULAR IMPLANTABLE DEVICE HAVING INTEGRATED ANCHOR MECHANISM - Devices, systems and methods are provided for an intravascular implantable device having an integrated anchor mechanism that can be deployed by compressing the anchor in an axial direction. Various embodiments address the various issues presented by the prior art and/or improve upon the prior art devices, methods and systems for anchoring an intravascular implantable device within a vessel. | 2011-01-06 |
20110004289 | METHODS AND APPARATUS FOR A STENT HAVING AN EXPANDABLE WEB STRUCTURE - The present invention provides a stent comprising a tubular flexible body having a wall with a web structure that is expandable from a contracted delivery configuration to deployed configuration. The web structure comprises a plurality of neighboring web patterns, where each web patterns is composed of adjoining webs, and the web patterns are interconnected. Each adjoining web comprises a central section interposed between two lateral sections to form concave or convex configurations. | 2011-01-06 |
20110004290 | HIGHLY FLEXIBLE STENT AND METHOD OF MANUFACTURE - Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding having interconnected struts joined at vertices, and having bridges connecting sections of the helical winding to each other. An annular ring can be provided at one or both ends of the helical winding, and the annular ring can have five extensions extending to connect to the helical winding. One of the extensions can connect to a bridge and another extension can connect to a vertex. The struts at the ends of the helical winding can have strut lengths that differ from the strut lengths of the struts in a central portion of the winding between the ends of the winding. | 2011-01-06 |
20110004291 | OSTIUM SUPPORT FOR TREATING VASCULAR BIFURCATIONS - A prosthesis is disclosed for placement across an ostium opening from a main body lumen to a branch body lumen. The prosthesis comprises a radially expansible support at one end, a circumferentially extending link at the other end and at least one frond extending axially therebetween. The circumferential link can comprise a catheter securement portion and a frond engagement portion. | 2011-01-06 |
20110004292 | OSTIUM SUPPORT FOR TREATING VASCULAR BIFURCATIONS - A prosthesis is disclosed for placement across an ostium opening from a main body lumen to a branch body lumen. The prosthesis comprises a radially expansible support at one end, a circumferentially extending link at the other end and at least one frond extending axially therebetween. | 2011-01-06 |
20110004293 | ENDOVASCULAR PLATFORMS FOR THE DIFFERENTIAL TARGETING OF MOLECULES TO VESSEL WALL AND VESSEL LUMEN - A drug delivering medical system intended for placement into a blood vessel is provided. The drug delivering medical system includes a stent device having a plurality of interconnected distinct strut elements comprising distinct strut element surfaces. At least some of the distinct strut surfaces are neither in contact with the lumen wall nor in contact with wall-contacting flow recirculation zones. The stent device releases at least one biologically active compound intended for distal delivery and provides sufficient surface area for delivering the required drug dose to a distal tissue. | 2011-01-06 |
20110004294 | FATIGUE-RESISTANT STENT - A fatigue-resistant implantable medical device. The fatigue-resistant implantable medical device includes a tubular stent. The tubular stent can have a laser-cut length and a shape-set length that is either longer or shorter than the laser-cut length. Such stents will tend to return to their laser-cut length when they are compressed for delivery. A stent that is shape-set longer than its laser-cut/delivery length that is deployed in a vessel that is shortened for stent delivery will tend to return to its shape-set length when the vessel returns to its neutral (i.e., elongated) length. Likewise, a stent that is shape-set shorter than its laser-cut/delivery length that is deployed in a vessel that is elongated for stent delivery will tend to return to its shape-set length when the vessel returns to its neutral (i.e., shortened) length. Such stents will experience reduced axial loading and reduced mean strain, thereby improving fatigue life. | 2011-01-06 |
20110004295 | Implant valve for implantation in a blood vessel - An implant valve for implantation in a blood vessel is comprised of a flexible tube and a hollow, substantially cylindrical support with a casing, expandable in diameter from an initial position to an implantation position. The support extends substantially coaxially over a part of the length of the tube along the inner wall of the tube. The casing of the support cooperates with the inner wall of the tube such that, in the implantation position, a first part of the tube can be formed into a rigid shell, which can be clamped substantially coaxially along the inner wall of a blood vessel. A second, axially contiguous part of the tube can then form a flexible, tubular valve body, which can extend substantially clear in the blood vessel. In an advantageous embodiment, the flexible tube comprises a vein turned inside out and the ends of the tube are connected to form a ring embracing the support. | 2011-01-06 |
20110004296 | Heart Valve Stent - A heart valve stent ( | 2011-01-06 |
20110004297 | TRANSLUMENAL APPARATUS, SYSTEM, AND METHOD - Methods, apparatus, and systems for altering the configuration of a heart valve. Methods, apparatus, and systems include the use of a cord delivered into the heart by a delivery catheter that can be manipulated by a receiving catheter so as to improve the heart valve function. | 2011-01-06 |
20110004298 | ANNULOPLASTY APPARATUS AND METHODS - An annuloplasty system for repairing a valve in a patient's heart comprises a surgical implant including a member having first and second end portions. The implant member further is configured and/or adapted to form a partial ring along a portion of one of the valve annulae of a patient's heart such as the mitral or tricuspid valve annulus. The implant member is axially elastic such that it can axially expand and contract and includes first and second anchors extending from the end portions of the implant member. The anchors are adapted to anchor the implant in tissue such as the mitral or tricuspid valve annulus. The system can facilitate tissue plication (e.g., of the posterior annulus of the mitral valve or the annulus of the tricuspid valve) and reinforcement of a valve annulus. | 2011-01-06 |
20110004299 | APPARATUS AND METHOD FOR REPLACING A DISEASED CARDIAC VALVE - An apparatus for replacing a diseased cardiac valve is movable from a radially collapsed configuration to a radially expanded configuration. The apparatus comprises an expandable support member and a prosthetic valve secured therein. The main body portion extends between first and second end portions and includes an outer circumferential surface, a circumferential axis extending about the circumferential surface, and a plurality of wing members spaced apart from one another by an expandable region. Each of the wing members includes first and second end portions and a flexible middle portion extending between the end portions. The second end portion is integrally formed with the main body portion. The first end portion is adjacent the circumferential axis and substantially flush with the outer circumferential surface in the radially collapsed configuration. The first end portion extends substantially radial to the outer circumferential surface in the radially expanded configuration. | 2011-01-06 |
20110004300 | PERCUTANEOUS AORTIC VALVE - The present invention provides a valve configured for insertion on the proximal and distal sides of a heart valve annulus to replace the heart valve of a patient. The valve comprises a first substantially annular portion adapted to be positioned on a proximal side of the annulus of a patient and a second substantially annular portion adapted to be positioned on a distal side of the annulus of a patient, wherein at least one of the first and second substantially annular portions is movable towards the other portion to a clamped position to clamp around the annulus. The second portion has a flow restricting portion extending therefrom and is movable between a first position to permit the flow of blood and a second position to restrict the flow of blood. In one embodiment, the valve has a suture joining the first and second portions to draw the first and second portions into closer proximity and a cinch member to secure the suture to maintain the first and second portions in the clamped position. In another embodiment, the first and second portions are connected by a first segment which biases the first and second portions toward the clamped position. | 2011-01-06 |
20110004301 | UV/VISIBLE LIGHT ABSORBERS FOR OPHTHALMIC LENS MATERIALS - Benzotriazole UV/Visible light-absorbing monomers are disclosed. The UV/Vis absorbers are particularly suitable for use in intraocular lens materials. | 2011-01-06 |
20110004302 | OPHTHALMIC SIZING DEVICES AND METHODS - An apparatus for sizing an intraocular lens and/or an ocular region of the eye of a subject, such as the anterior chamber, contains a sizing device and a measurement device. In one embodiment, the sizing device comprises a first leg having a first contact portion for operably engaging the ocular portion and a second leg having a second contact portion for operably engaging the ocular portion. The sizing device has a test geometry when placed within the ocular portion. The measurement device is adapted for determining a dimension of the sizing device based at least in part on the test geometry. The sizing device may also have a reference geometry when the sizing device in a reference condition. In certain embodiments, the difference between the reference geometry and the test geometry may be used for sizing the intraocular lens and/or the ocular portion. | 2011-01-06 |
20110004303 | GLARE REDUCING ROUGH SURFACES - An intraocular lens for insertion into a capsular bag in order to focus incoming light toward a retina and process for manufacturing thereof along with concomitant reduced glare and improved vision provides for a center lens portion of a lens for focusing incoming light toward the retina and the surrounding lens portion for mounting the lens within the capsular bag. A surface roughness disposed on the surrounding lens portion is provided for reducing the glare due to non-focused light directed toward the retina from the intraocular lens with the roughness having a roughness level of between about Ra 45 and about Ra 350. | 2011-01-06 |
20110004304 | CULTURING RETINAL CELLS AND TISSUES - Disclosed are various methods and bioreactor devices for culturing retinal cells and/or tissues. The bioreactor devices may, in certain embodiments, include a microchannel network, a scaffold for culturing neuroretinal cells, and a porous membrane separating the microchannel network from the scaffold. | 2011-01-06 |
20110004305 | ELEVATED IMPLANT FOR THE RECONSTRUCTION OF MENISCUS DEFECTS OR PARTIAL MENISCUS DEFECTS - An implant for reconstructing meniscus defects or partial meniscus defects includes an elevated molding with a femoral condylar contact area, a tibial condylar contact area and an articular capsule contact area, in the manner of an artificial meniscus or artificial partial meniscus with a contour of an outer area that is substantially the same as a natural meniscus or partial meniscus, wherein at least one additional elevation is formed on the outer area of the elevated molding. | 2011-01-06 |
20110004306 | DEVICE AND METHOD FOR TREATMENT OF INCISION OR HERNIA - Devices and methods for treating an abdominal incision or hernia are described. An implant for the restoration or prophylactic treatment of an abdominal wall comprises an elongate element and at least one sheet connected to the elongate element along a longitudinal axis of the elongate element. The elongate element is positioned along the line of incision, and the at least one sheet is secured to the abdominal muscles surrounding the incision. | 2011-01-06 |
20110004307 | FUSION DEVICE, SYSTEMS AND METHODS THEREOF - The spinal fusion device ( | 2011-01-06 |
20110004308 | EXPANDING INTERVERTEBRAL DEVICE AND METHODS OF USE - Disclosed is a spinal stabilization device having a plurality of elongate arms having a distal end portion and a proximal end portion, wherein the elongate arms define an interior volume between the distal end portion and the proximal end portion; at least one limit band coupled circumferentially to one or more of the plurality of elongate arms; and a tensioning element positioned within the interior volume. The plurality of elongate arms can transition from a constrained, delivery configuration that is radially contracted and axially elongated to a relaxed, deployment configuration that is radially expanded and axially shortened. | 2011-01-06 |
20110004309 | Method and arrangement at implants preferably for a human intervertebral and such implant - In an arrangement for production of implant consisting of biocompatible material and intended for a vertebral disk, preferably intervertebral disk in the human body, the condition (state) of the disk is established by aids of condition establishing means and parameters. A first information created by aid of the means and parameters is arranged to control computer equipment for production of a simulation model of the disk in question with surrounding vertebras. A second information created by the computer equipment in dependency of the simulation incorporates or consists of information about the outer volume and design of the implant put in relation to the present alteration of or in the disk. The second information is arranged to initiate or contribute to the control of one or more equipments for production of the implant. In this manner, it is possible to arrange a technical arrangement and method for an individually adapted implant. | 2011-01-06 |
20110004310 | Lordotic interbody spinal fusion implants - The present application is directed to interbody spinal fusion implants having a structural configuration that provides for the maintaining and creating of the normal anatomic angular relationship of two adjacent vertebrae of the spine to maintain and create spinal lordosis. The spinal fusion implants are sized to fit within the disc space created by the removal of disc material between two adjacent vertebrae and conform wholly or in part to the disc space created. The spinal fusion implants of the present invention have upper and lower surfaces that form a support structure for bearing against the end plates of the adjacent vertebrae. The upper and lower surfaces are disposed in a converging angular relationship to each other such that the implants have an overall “wedged-shape” in an elevational side view. The angular relationship of the upper and lower surfaces places and maintains the vertebrae adjacent to those surfaces in an angular relationship to each other, creating and maintaining the desired lordosis. | 2011-01-06 |
20110004311 | SHAPED IMPLANTS FOR TISSUE REPAIR - Shaped constructs for repair of a defect in a body part or tissue of a subject are discussed herein. More specifically, implants suitable for delivery to a subject, such as a subject having a defect in a body part or body tissue, are discussed. Even more specifically, implants for intervertebral disc repair comprising corticocancellous bone, which can extend into the nucleus pulposus of an intervertebral disc and can be integrally attached to the annulus fibrosus of the disc to keep the implant in position, are described. Also, implants for meniscal repair comprising corticocancellous bone, which can extend from the outer edge of the meniscus to the inner region of the meniscus and can be integrally attached to the meniscal rim to keep the implant in position, are described. Implants for the repair of defects in bone, cartilage, and fibrocartilage are further described. Further described are methods for making such implants and for delivering the implants to a defect in a body part or body tissue of a subject. | 2011-01-06 |