31st week of 2009 patent applcation highlights part 46 |
Patent application number | Title | Published |
20090192524 | SYNTHETIC REPRESENTATION OF A SURGICAL ROBOT - A synthetic representation of a robot tool for display on a user interface of a robotic system. The synthetic representation may be used to show the position of a view volume of an image capture device with respect to the robot. The synthetic representation may also be used to find a tool that is outside of the field of view, to display range of motion limits for a tool, to remotely communicate information about the robot, and to detect collisions. | 2009-07-30 |
20090192525 | TAPE-BASED SKIN TREATMENT - A SAFE AND QUICK ALTERNATIVE TO SKIN RENEWAL - A skin renewal sheet for exfoliating skin includes a flexible backing layer, a skin-friendly pressure-sensitive adhesive layer disposed on one side of the backing layer and a release layer disposed on the skin friendly pressure sensitive adhesive layer wherein the pressure sensitive adhesive layer has a 180° peel force of from about 0.5 lbs/in. to about 5.0 lbs/in. | 2009-07-30 |
20090192526 | Apparatus and method for concurrently forming a gastroesophageal valve and tightening the lower esophageal sphincter - An apparatus enables concurrent restoration of a gastroesophageal valve and tightening of the lower esophageal sphincter. The apparatus comprises a longitudinal member having a distal end arranged to be received within a stomach, a tissue shaper at the distal end of the longitudinal member that forms a gastroesophageal valve from stomach tissue, and a tissue gatherer that gathers fundus tissue at or aboral to the gastroesophageal junction to reduce an esophageal opening into the stomach and tighten the lower esophageal sphincter. A fastener deployer then deploys at least one fastener pair to maintain both the restored gastroesophageal valve and the tightened lower esophageal sphincter. | 2009-07-30 |
20090192527 | Parietal anchoring tool and device, in particular for laparoscopic or coelioscopic surgery - The invention relates to a tool for parietally anchoring a living being's organ ( | 2009-07-30 |
20090192528 | METHOD AND DEVICE FOR HERNIA REPAIR - A device for repairing a hernia defect in a patient, the device having a biocompatible mesh material having a treated surface and a tissue composition coated on at least a portion of the treated surface, where the tissue composition originates from the patient. A method of preparing a surgical mesh for repairing a hernia defect, comprises placing a tissue specimen into a container, centrifuging the container to separate the specimen into at least two fractions, then drawing a selected fraction from the container, treating a surface of a biocompatible mesh and coating the surface-treated biocompatible mesh with the selected fraction. | 2009-07-30 |
20090192529 | SOFT TISSUE REATTACHMENT MECHANISM - Among other things, apparatus and methods for reattaching soft tissue to bone are disclosed. In one embodiment, a monolithic anchor having a head flexibly attached to a stem including ridges or grooves is provided. A locking member may be placed over the stem, which has one or more pawls to engage the ridges or grooves to inhibit the locking member from coming off of the stem. A tube may be provided for access to the surgical location. With the tube placed through soft tissue and cortical bone or other access, the anchor with the head pivoted to be parallel with or along the stem may be placed through holes in the soft tissue and cortical bone. The head is turned transverse to the stem, preventing the head from passing back through the cortical bone. The locking member is placed over the stem to hold the soft tissue to the bone. | 2009-07-30 |
20090192530 | FORTIFIED MESH FOR TISSUE REPAIR - A mesh to repair a hole in a muscle wall includes a resilient mesh body and fortifying structure such as mesh portions of thicker weave than other portions, or strengthening members that can be engaged with the mesh and then removed from the mesh once the mesh is place over the hole. The same principles can be applied to a plug that is engaged with the mesh for filling the hole. | 2009-07-30 |
20090192531 | METHODS AND DEVICES FOR TREATING OBESITY AND GERD BY INTUSSUSCEPTING A PORTION OF STOMACH TISSUE - Described here are devices and methods for intussuscepting a portion of stomach tissue. Typically the intussusception is created at a position near, but distal to the gastroesophageal junction, and a pouch capable of storing a volume (from about 0 cc up to about 100 cc) is created proximal the intussuscepted tissue. In this way, the amount of food that may be ingested is reduced, helping to ameliorate GERD symptoms, and aiding in weight loss efforts. Some of the devices described here include an expandable member and at least one suction inlet. In these devices, the expandable member is expanded to create a proximal cavity into which the stomach tissue is pulled (e.g., using suction), thereby creating the intussusception. | 2009-07-30 |
20090192532 | IMPLANT FOR PARASTOMAL HERNIA - An implant for the prevention or treatment of a hernia in the proximity of an organ stoma formed in an abdominal wall includes a porous structure having a surface intended to face the abdominal cavity covered by a first film of anti-adhesive material. The porous structure includes a first part intended to be in contact with a stoma organ and having a first thickness, and a second part having a second thickness greater than the first thickness, the first part including a surface intended to face the abdominal wall covered by a second film of anti-adhesive material. | 2009-07-30 |
20090192533 | METHODS AND DEVICES FOR DIAGNOSING PERFORMANCE OF A GASTRIC RESTRICTION SYSTEM - Methods and devices are provided for diagnosing performance of a gastric restriction system. In general, the methods and devices can enable patients, health care providers, and others to use pressure data as a feedback mechanism to monitor efficacy of an implantable restriction device and to identify, train, and/or prescribe treatment plan options. Pressure data monitoring can be used locally and/or remotely to monitor a restriction in a patient and compare gathered pressure data with a typical pressure of the restriction. Based on the results of the comparison, possible problems related to the patient and the restriction can be identified and diagnosed with possible cause(s) and solution(s). Notice of any detected possible problems, causes, and/or solutions can be provided to a user. | 2009-07-30 |
20090192534 | SENSOR TRIGGER - Methods and devices for effecting a gastric restriction system are disclosed. In one exemplary embodiment, a restriction system for forming a restriction in a patient is provided and can include an implantable restriction device and at least one implantable sensor that is in communication with the restriction device. In general, the implantable restriction device can be adjustable and can be configured to form a restriction in a patient. The implantable sensor(s) can be defaulted to a dormant power usage mode and can have a triggering mechanism that is configured to place the sensor(s) in a use configuration upon the occurrence of a triggering event. | 2009-07-30 |
20090192535 | Swallowable Self-Expanding Gastric Space Occupying Device - Disclosed is a swallowable self-expanding gastric space occupying device and related methods of making and using the device to control obesity. The device has a membrane through which gastric liquid can pass, wherein the membrane provides an enclosure volume separated from the gastric environment by the membrane. A plurality of self-expanding components is contained in the enclosure volume, so that the components expand in volume upon contact with the gastric fluid, thereby expanding the device from an unexpanded volume to an expanded volume. Composite membranes provide the ability to precisely control how and when the membrane degrades in the stomach, to release the self-expanding components from the enclosure and to ensure that the released pieces are sufficiently small to not obstruct any portion of the gastrointestinal system. | 2009-07-30 |
20090192536 | SYSTEM AND METHOD FOR DELIVERING AND DEPLOYING AN OCCLUDING DEVICE WITHIN A VESSEL - A system and method for deploying an occluding device that can be used to remodel an aneurysm within the vessel by, for example, neck reconstruction or balloon remodeling. The system comprises an introducer sheath and an assembly for carrying the occluding device. The assembly includes an elongated flexible member having an occluding device retaining member for receiving a first end of the occluding device, a proximally positioned retaining member for engaging a second end of the occluding device and a support surrounding a portion of the elongated flexible member over which the occluding device can be positioned. | 2009-07-30 |
20090192537 | Cutting Balloon Catheter Having Increased Flexibility Regions - A cutting balloon catheter and method of using the same. The cutting balloon catheter may include a catheter shaft having a balloon coupled thereto. One or more cutting members or blades may be coupled to the balloon. The balloon may include one or more discrete points or areas of flexibility to enhance flexibility of the cutting balloon catheter. A break in the one or more cutting members may be aligned with the one or more discrete points of flexibility in the balloon. | 2009-07-30 |
20090192538 | SAFETY SCALPEL HANDLE - A scalpel handle includes a sliding shield to block the blade tip or surround the blade when the scalpel is not in use. The shield is advantageously slidable from an extended position to a withdrawn position, wherein the shield is substantially within the handle. Consequently, the user's hand grasps only onto the handle, and not the shield. This helps to provide a more solid feel, similar to a conventional scalpel handle. When in the withdrawn position, the shield avoids interfering with cutting or puncturing blade movements. | 2009-07-30 |
20090192539 | Methods and Devices for altering blood flow through the left ventricle - An element is expanded in the left ventricle to isolate part of the left ventricle. The element has a generally convex outer surface and an apex which together define a desired geometry of the left ventricle. The isolated part of the wall of the left ventricle may be left so that the wall naturally forms around the element or the isolated portion of the ventricle may be evacuated and/or filled. The element may also be used to isolate part of the left ventricle containing a ventricular septal defect or other perforation or opening in the ventricular wall. | 2009-07-30 |
20090192540 | SYSTEMS AND METHODS RELATING TO ASSOCIATING A MEDICAL IMPLANT WITH A DELIVERY DEVICE - The present invention provides devices and methods for associating an implantable sling with a delivery device for delivering the sling to an anatomical location in a patient. | 2009-07-30 |
20090192541 | METHODS AND DEVICES FOR PREDICTING PERFORMANCE OF A GASTRIC RESTRICTION SYSTEM - Methods and devices are provided for predicting performance of a restriction system for a patient. In general, the methods and devices can allow detection and prediction of a trajectory of a particular patient attribute, such as weight loss. Using previously gathered data values, data values defining a future outcome can be predicted and compared with a desired future outcome. If the future outcome deviates from the desired future outcome, one or more corrective actions can be suggested to a patient and/or a health care provider to help align the patient's treatment plan with the desired future outcome rather than the currently predicted future outcome. | 2009-07-30 |
20090192542 | SINGLE BALLOON RIPENING DEVICE WITH NOVEL INSERTER AND INFLATOR - An improvement on the extra-amniotic balloon and technique of placement is disclosed. It involves a large capacity balloon, modified to efficiently place pressure on the cervix, and markers for ease and of placement. The malleable introducing stylet allows for safe and easy insertion, either manually or visually, through a cervix that is 0.5 cm or more in dilation. The optional traction collar can aid in more efficiently placing pressure on the cervix. The automatic pump for instillation of the fluid has a forward and reverse mode to allow for deflation and repositioning of the balloon if placement is less than optimal. This process can be performed by a physician or a nurse, already certified in the placement of fetal scalp electrodes or intrauterine pressure catheters. Additionally, the procedure can be performed by one person. | 2009-07-30 |
20090192543 | RETRIEVABLE IVC FILTER - Retrievable vena cava filters for filtering blood clots within a vessel are disclosed. A retrievable vena cava filter in accordance with an exemplary embodiment of the present invention may include a plurality of elongated filter legs each having a hook portion configured to engage the vessel wall, and an expandable member releasably connected to the filter. In certain embodiments, the expandable member may comprise a bendable member and several tubular members, or a coiled wire. | 2009-07-30 |
20090192544 | METHOD OF IMPROVED VEIN CLOSURE - There are disclosed methods of vein closure. In an embodiment, a method includes elevating a leg of a patient during a vein closure procedure so as to effect substantial emptying of the vein. The method also includes applying radio-frequency energy to a vein within the leg of the patient to cause the vein closure. In another embodiment, a method includes elevating a leg of a patient during a vein closure procedure within a range of about 30 degrees to about 45 degrees from a horizontal position. The method also includes applying radio-frequency energy to a vein within the leg of the patient. In one embodiment, a method includes elevating a leg, and emptying of a segment of the vein prior to applying radio-frequency energy. In another embodiment, the method includes elevating a leg of a patient, and applying energy to a vein. Other embodiments are also disclosed. | 2009-07-30 |
20090192545 | Curved suture anchor guide and method of use - A rigid, curved and hollow guide that can be used to facilitate a variety of arthroscopic surgeries is provided as well as a method of using the guide. In one embodiment, the guide ( | 2009-07-30 |
20090192546 | FENESTRATED SUTURE ANCHOR AND METHOD FOR KNOTLESS FIXATION OF TISSUE - A fenestrated suture anchor for fixation of tissue to bone. In a preferred embodiment, the suture includes an implant, such a swivel implant with a forked tip for capturing suture. The implant is secured in a hole in bone by advancing a fixation device, such as a cannulated interference screw, to engage and fully seat the implant. The cannulated fixation device is provided with a plurality of openings or fenestrations of various dimensions and geometries to provide multiple pathways through the anchor (i.e., though the interior of the body and through the fenestrations) to allow blood to flow to increase the healing zone, for example, for rotator cuff repair, while also promoting bone in-growth. | 2009-07-30 |
20090192547 | INFANT CHEW TOY - An infant chew toy apparatus includes an elongate handle and a flange or other lateral member disposed on the handle. The flange extends laterally from the handle. A protrusion is disposed on the flange. The protrusion may comprise a nipple, and may be oriented directionally opposite of and parallel to the handle. The flange may be disposed on an end of the handle, with another flange disposed on the opposite handle end. The apparatus is designed to make it convenient for infants to grip, chew, and pick up the apparatus, and portions of it may be constructed of suitably durable plastic or other material for teething purposes, with other portions constructed of softer material. | 2009-07-30 |
20090192548 | Pedicle-laminar dynamic spinal stabilization device - Apparatus, systems and methods for decompression and dynamic stabilization of the vertebrae. A flexion construct is formed from a medial loop of a cylindrical member in a first plane that is generally parallel to the long axis of the member, and two outlying loops, generally residing in a common second plane that is generally parallel to the long axis of the member and generally perpendicular to the first plane formed by the medial loop. The medial loop and outlying loops of the flexion construct may aid in controlling distraction, compression and flexion of the assembly. Multiple level constructs may include multiple sets of loops, one set for each spinal level. The member may also include two legs that terminate in hooks or include a straight portion for attachment by another attachment means. A protective sleeve may be used between the member and any attachment means. | 2009-07-30 |
20090192549 | BONE PLATING SYSTEM - A bone plating system has a plate and a locking element. The plate has a bone screw aperture defined by a sidewall including first and second substantially planar segments. The locking element is coupled to the plate and at least partially positioned in the aperture. The locking element has an external geometry defining first and second substantially planar surfaces and an internal geometry for receiving a head of a bone fastener and preventing the bone fastener from backing out of the plate. The locking element is expandable from a first state to a second state. In the first state the locking element is permitted to articulate relative to the plate. In the second state the first and second substantially planar surfaces of the locking element engage the first and second substantially planar segments of the aperture sidewall, respectively, to prevent relative movement between the locking element and the plate. | 2009-07-30 |
20090192550 | BONE PLATING SYSTEM - A bone plating system includes a plate member and a first bone screw. The plate member defines a longitudinal axis and has a top surface and a bottom surface. The plate member further defines an elongated hole extending between the top surface and the bottom surface with a width in a direction generally perpendicular to the elongated axis and a length with a greater dimension in a direction generally parallel to the elongated axis. The elongated hole is defined by a sidewall having a spherical cross section in the direction generally perpendicular to the elongated axis. The sidewall has a threading. The first bone screw has a threaded and spherical head for threadably engaging the elongated hole. The threading extends completely around the sidewall of the elongated hole such that the first bone screw may threadably engage the elongated hole anywhere along the length. | 2009-07-30 |
20090192551 | Facet Fixation Prosthesis - A facet screw system for surgical implantation into bone tissue having a shaft, a compression member and a washer. The shaft includes a shaft having a bone engaging portion and a compression member engaging portion. The compression member includes a spherical head portion having a recess for engaging with a driving instrument, and an elongated coupling portion having internal threads for coupling with the compression member engaging portion of the shaft and a washer coupled to the spherical head portion of the compression member and having a plurality of bone engaging protrusions. The washer is adapted to be polyaxially rotatable with respect to the compression member. | 2009-07-30 |
20090192552 | OSTEOPORATIC SCREW AND EXPANSION SLEEVE - The invention is a bone screw apparatus. The bone screw apparatus has two specialized functions for stabilizing the screw within a bone. The first is a mechanical structure that anchors the screw within a bone and the second is a structure that allows injection of bone cement through the screw assembly and into the interior structure of the bone. The anchoring mechanism functions by an expandable member that slides concentrically over the shaft of the screw. When the expandable member is forced over a portion of the screw shaft with an enlarged diameter, the expandable member extends radially from the screw shaft, and the bone screw is anchored to the interior structure of the bone. The injecting function of the bone screw apparatus functions through the use of a hollow core within the screw shaft. The hollow core of the screw shaft has an inlet at the top of the shaft and at least one outlet near the tip of the screw shaft. Once the screw shaft is inserted into the interior structure of a bone, bone cement may be injected into the inlet at the top of the screw shaft. The bone cement travels through the hollow core of the screw shaft and is extruded out the holes near the tip of the screw shaft. The bone cement fills the void spaces within the bone structure and strengthens the bone. | 2009-07-30 |
20090192553 | ANTI-BACKOUT MECHANISM - Methods and devices for locking a fastener in a thru-bore are provided herein. In one exemplary embodiment, a spinal anchor is provided that includes a bone engaging fastener, an anti-backout mechanism, and a locking mechanism. The anti-backout mechanism can be movable between a retracted position in which it is disposed within the fastener and a deployed position in which is extends from the bone engaging fastener. The locking mechanism can be matable to the bone engaging fastener and can be configured to move the anti-backout mechanism from the retracted position to the deployed position. In the deployed position, the anti-backout mechanism can prevent the bone engaging fastener from backing out of a thru-bore in a spinal plate. | 2009-07-30 |
20090192554 | BIOABSORBABLE BLOCK COPOLYMER - A bioabsorbable polyurethane block copolymer with having hard and soft segments is formed by the reaction between a diisocyanate such as lysine ethyl ester diisocyanate and a mixture of (i) an aromatic amide or an amino acid derivative and (ii) a polyether glycol and/or an absorbable elastomeric polymer derived from the reaction between dialkylene glycol and a cyclic bioabsorbable monomer such as trimethylene carbonate, caprolactone, or dioxanone. | 2009-07-30 |
20090192555 | FIXATION OF IMPLANTABLE PULSE GENERATORS - Systems and techniques for improving the fixation of implantable pulse generators. In one aspect, a device includes an implantable pulse generator that comprises electrical circuitry configured to generate an electrical pulse and a biocompatible casing that houses the electrical circuitry and on which a collection of electrodes and a collection of fixation elements are mounted. The electrodes are in electrical contact with the electrical circuitry and the fixation elements increase the surface area of the biocompatible casing to reduce the likelihood that the biocompatible casing shifts after implantation; | 2009-07-30 |
20090192556 | SLEEP STAGE DETECTION - Therapy delivery to a patient may be controlled based on a determined sleep stage of the patient. In examples, the sleep stage may be determined based on a frequency characteristic of a biosignal indicative of brain activity of the patient. A frequency characteristic may include, for example, a power level within one or more frequency bands of the biosignal, a ratio of the power level in two or more frequency bands, or a pattern in the power level of one or more frequency bands over time. A therapy program may be selected or modified based on the sleep stage determination. Therapy may be delivered during the sleep stage according to the selected or modified therapy program. In some examples, therapy delivery may be controlled after making separate determinations of a sleep stage based on the biosignal and another physiological parameter, and confirming that the sleep stage determinations are consistent. | 2009-07-30 |
20090192557 | METHODS AND SYSTEMS OF TREATING PANCREATITIS PAIN CAUSED BY SPHINCTER OF ODDI DYSFUNCTION - Methods and systems of treating a patient with pancreatitis pain include providing a stimulator, configuring one or more stimulation parameters to control sphincter of Oddi function, programming the stimulator with the one or more stimulation parameters, generating a stimulus configured to control sphincter of Oddi function with the stimulator in accordance with the one or more stimulation parameters, and applying the stimulus with the stimulator to one or more stimulation sites in accordance with the one or more stimulation parameters. | 2009-07-30 |
20090192558 | METHODS AND SYSTEMS OF TREATING PANCREATITIS PAIN - Methods and systems of treating a patient with pancreatitis pain include providing a stimulator, configuring one or more stimulation parameters to treat pancreatitis pain, programming the stimulator with the one or more stimulation parameters, generating a stimulus configured to treat pancreatitis pain with the stimulator in accordance with the one or more stimulation parameters, and applying the stimulus with the stimulator to one or more stimulation sites in accordance with the one or more stimulation parameters. | 2009-07-30 |
20090192559 | Cordless Internal Defibrillator - A single-handle cordless internal defibrillator includes a pair of paddles, and a pair of electrodes that are respectively connected to a first-end portion of the pair of paddles. The pair of paddles has a second-end portion in communication with a single-handle, with a least one paddle of the pair of paddles being pivotable about a pivot arranged between the one paddle and the single-handle. A regulator arm in communication with the pivot adjusts the pivot of at least one paddle about the pivot so that the distance between the electrodes is variable by moving the regulator arm, and defibrillator circuitry is arranged within the single-handle. A dual-handle structure also provides tangle-free and clutter-free applications as the defibrillator circuitry is self-contained in the handle/handles or paddles of the defibrillator, eliminating the need for long cables which obstruct and can contaminate an operating room. | 2009-07-30 |
20090192560 | CONFIGURABLE INTERMITTENT PACING THERAPY - This document discusses, among other things, an apparatus comprising at least one implantable cardiac depolarization sensing circuit, an electrical stimulation circuit, and a pacing mode controller. The implantable cardiac depolarization sensing circuit is configured to obtain a sensed depolarization signal from a ventricle and the electrical stimulation circuit is configured to provide pacing electrical stimulation energy to at least one implantable ventricular electrode. The pacing mode controller delivers pacing therapy according to a first pacing mode that is a normal operating mode, and delivers pacing therapy according to second and third pacing modes. The second and third pacing modes increase mechanical stress on at least a particular portion of the ventricle as compared to the pacing therapy delivered during the first pacing mode. The pacing mode controller alternates between the second and third pacing modes when switched from the normal operating mode to a stress augmentation mode. | 2009-07-30 |
20090192561 | On-again, off-again physiologic-demand heart pacing - A method of intentional on-again, off-again physiologic-demand heart pacing associated with at least one of (a) an implantable, and (b) an external, controllable/adjustable heart-pacing device having on and off states. The method involves gathering categories of a person's physiologic data, including ECG and heart-sound data, which are (a) relevant to that person's heart's pumping and filling functionalities, and (b) suitable for computing a selected acoustic cardiographic value; and based on such gathering and computing, and using a controlled combination of on and off states in the pacing device, recurrently adjusting the operation of that device, as necessary, so as to maintain a minimum difference between such a computed acoustic cardiographic value and a predetermined, reference acoustic cardiographic value. | 2009-07-30 |
20090192562 | CARDIAC RESYNCHRONIZATION VIA LEFT VENTRICULAR PACING - The invention is directed to techniques for providing cardiac resynchronization therapy by synchronizing delivery of pacing pulses to the left ventricle with intrinsic right ventricular depolarizations. An implantable medical device measures an interval between an atrial depolarization and an intrinsic ventricular depolarization is measured. In various embodiments, the intrinsic ventricular depolarization may be an intrinsic right or left ventricular depolarization. The implantable medical device delivers pacing pulses to the left ventricle to test a plurality of pacing intervals. The pacing intervals tested may be within a range around the measured interval between the atrial depolarization and the intrinsic ventricular depolarization. One of the pacing intervals is selected based on a measured characteristic of an electrogram that indicates ventricular synchrony. For example, the pacing interval may be selected based on measured QRS complex widths and/or Q-T intervals. The implantable medical device paces the left ventricle based on the selected pacing interval. | 2009-07-30 |
20090192563 | METHOD AND APPARATUS FOR ADJUSTING CARDIAC EVENT DETECTION THRESHOLD BASED ON DYNAMIC NOISE ESTIMATION - An implantable cardiac rhythm management (CRM) device includes a sensing and detection circuit that senses at least one cardiac signal and detects cardiac electrical events from the sensed cardiac signal using a detection threshold that is adjusted based on a dynamic noise estimation. The sensed cardiac signal is filtered to produce a filtered cardiac signal having a signal frequency band and a noise signal having a noise frequency band. The noise frequency band is substantially different from the signal frequency band. A dynamic noise floor is produced based on the noise signal and used as the minimum value for the detection threshold. A cardiac electrical is detected when the amplitude of the filtered cardiac signal exceeds the detection threshold. | 2009-07-30 |
20090192564 | Changeable electrode polarity stimulation by an implantable medical device - We disclose a method of treating a medical condition in a patient using an implantable medical device including coupling at least a first electrode and a second electrode to a cranial nerve of the patient, providing a programmable electrical signal generator coupled to the first electrode and the second electrode, generating a first electrical signal with the electrical signal generator, applying the first electrical signal to the electrodes, wherein the first electrode is a cathode and the second electrode is an anode, reversing the polarity of the first electrode and the second electrode, yielding a configuration wherein the first electrode is an anode and the second electrode is a cathode, generating a second electrical signal with the electrical signal generator, applying the second electrical signal to the electrodes, reversing the polarity of the first electrode and the second electrode, yielding a configuration wherein the first electrode is a cathode and the second electrode is an anode, generating a third electrical signal with the electrical signal generator, and applying the third electrical signal to the electrodes. Each of the electrical signals can independently contain one or more pulses or one or more bursts. The number of pulses need not be equal between any two of the electrical signals. | 2009-07-30 |
20090192565 | STIMULATION OF THE STOMACH IN RESPONSE TO SENSED PARAMETERS TO TREAT OBESITY - A neurostimulation kit and a method of treating a patient are provided. The kit comprises a stimulation backing that includes a flat, electrically insulative, body having a pair of opposing first and second planar surfaces, and an electrode affixed to the first surface of the insulative body. The stimulation backing is implanted within a patient and affixed therein to place the electrode into contact with a tissue surface. The kit comprises a neurostimulator including a housing and stimulation circuitry contained within the housing. The neurostimulator is implanted within the patient by affixing the housing to the second surface of the insulative body, such that the stimulation circuitry is electrically coupled to the electrode. | 2009-07-30 |
20090192566 | Device for and Method of Generating a Baroreflex Response - This patent relates to a device for and method of stimulating the carotid sinus baroreceptors to achieve a restoration or resetting of baroreflex response and natural blood pressure modulation. The stimulation may consist of low amplitude, wide bandwidth signals that produce a stochastic resonance effect. The ultimate affect is blood pressure modulation within a reduced range including establishment of thresholds at which baroreceptors trigger normal central nervous system functions. | 2009-07-30 |
20090192567 | Method, Apparatus and System for Bipolar Charge Utilization During Stimulation by an Implantable Medical Device - We disclose a method, apparatus, and system of treating a medical condition in a patient using an implantable medical device. A first electrode is coupled to a first portion of a cranial nerve of the patient. A second electrode is coupled to a second portion of the cranial nerve of the patient. A first electrical signal is provided to the first and second electrodes. The first electrical signal is provided in a first polarity configuration in which the first electrode functions as an anode and the second electrode functions as a cathode. Upon termination of the first electrical signal, the anode and cathode each comprise a first accumulated energy. A second electrical signal is provided to the first and second electrodes, in which the second electrical signal includes at least a portion of the first accumulated energy. | 2009-07-30 |
20090192568 | METHODS AND SYSTEMS FOR TREATING SEIZURES CAUSED BY BRAIN STIMULATION - Methods for treating seizures caused by brain stimulation include providing a stimulator, programming the stimulator with one or more stimulation parameters configured to treat a medical condition, applying at least one stimulus with the stimulator to a stimulation site within the brain of a patient in accordance with the one or more stimulation parameters, and monitoring the patient for a seizure caused by the at least one stimulus. | 2009-07-30 |
20090192569 | CORTICAL ELECTRODE ARRAY AND METHOD FOR STIMULATING AND RECORDING BRAIN ACTIVITY - An electrode device and a method of installing the electrode device in the vicinity of the brain. The electrode device includes a plurality of electrode assemblies, each with at least one electrode lead, extending from a common base. The base is configured to be positioned on an outside of the patient's cranium with each electrode assembly projecting individually through a hole in the patient's cranium such that the electrode lead is in the vicinity of the brain. The method of installation includes carving a recess out of the patient's cranium and inserting the base therein. Each of the electrode assemblies are placed in their respective holes in order to stimulate, monitor or record neurological activity. The electrode device may be used over long periods of time for chronic treatment or recording. | 2009-07-30 |
20090192570 | METHODS AND SYSTEMS OF TREATING ISCHEMIA PAIN IN VISCERAL ORGANS - Methods and systems of treating a patient with ischemia pain include providing a stimulator, configuring one or more stimulation parameters to treat ischemia pain in a visceral organ, programming the stimulator with the one or more stimulation parameters, generating a stimulus configured to treat ischemia pain with the stimulator in accordance with the one or more stimulation parameters, and applying the stimulus with the stimulator to one or more stimulation sites in accordance with the one or more stimulation parameters. | 2009-07-30 |
20090192571 | DEVICE WITH A BASE BODY - On a device | 2009-07-30 |
20090192572 | Bidirectional Communications Between A Generator And Sensors Or Actuators Of A Lead For An Active Implantable Medical Device - An active implantable medical device including bidirectional communications between a generator and sensors or actuators located at the distal extremity of a lead. A lead ( | 2009-07-30 |
20090192573 | COUPLING ELEMENT - An element ( | 2009-07-30 |
20090192574 | ANTENNA FOR AN IMPLANTABLE MEDICAL DEVICE - An apparatus and method for enabling far-field radio-frequency communications with an implantable medical device in which an antenna is embedded within a dielectric compartment of the device. A helical antenna may be employed to save space while still permitting far-field telemetry over a desired range of frequencies. | 2009-07-30 |
20090192575 | THERMAL MANAGEMENT OF IMPLANTABLE MEDICAL DEVICES - Systems and techniques for thermal management of implantable medical devices. In one aspect an implantable device includes an active component configured to perform medical activities, a charging component configured to convert energy from outside a body in which the implantable device is implanted into potential energy, and a thermal barrier between the charging component and the active portion. The thermal barrier thermally isolates the charging component from the active portion so that thermal resistance between the charging component and the active component is above the thermal resistance between the charging component and the body. | 2009-07-30 |
20090192576 | MEDICAL ELECTRICAL LEAD - A medical device lead is presented. One embodiment of the claimed invention includes a lead body, a conductor, and a flexible component. The lead body includes a proximal end and a distal end. The conductor is coupled to the lead body. A sleeve is coupled to the distal end of the lead body. The flexible component is coupled to the distal end of the sleeve. The distal end of the flexible component includes an outer diameter that is greater than the outer diameter of the proximal end. | 2009-07-30 |
20090192577 | MEDICAL ELECTRICAL LEAD WITH COATED CONDUCTOR - A medical electrical lead includes a conductor having at least one layer of a parylene coating formed from a polyxylylene based polymer. The conductor can be a cable or a coiled conductor including one or more individual conductive filaments. The parylene coating may be provided over the individual conductive filaments or provided over an outer periphery of the conductor formed from the individual conductive filaments. Additionally, the parylene coating can be provided in more than one location. Lead bodies having reduced outer diameters without compromising the desired physical properties of a medical electrical lead may be constructed. | 2009-07-30 |
20090192578 | HEADER OVER-MOLDED ON A FEEDTHROUGH ASSEMBLY FOR AN IMPLANTABLE DEVICE - A header assembly for connecting a conductor terminating at a body organ with an implantable medical device is described. The header assembly comprises a base plate, a feedthrough subassembly disposed in the base plate and comprising a ceramic-to-metal seal with first and second feedthrough wires passing through the ceramic-to-metal seal; a first electrically conductive terminal connected to a distal end of the first feedthrough wire and having a first lead opening sized to receive a first portion of a lead for the conductor; a second electrically conductive terminal connected to a distal end of the second feedthrough wire and having a second lead opening sized to receive a second portion of the lead for the conductor; a body of polymeric material molded in a two-part construction to encase the conductive terminals and their feedthrough wires except for a first bore communicating from outside the polymeric body to the first and second lead openings aligned in a first co-axial relationship. Preferably, the polymeric body comprises a first polymeric material such as Techothane® or Polysulfone® encasing the terminals except the bore and an epoxy as a second polymeric material molded over the first polymeric material. | 2009-07-30 |
20090192579 | IMPLANTATION METHODS, SYSTEMS AND TOOLS FOR INTRAVASCULAR IMPLANTABLE DEVICES - Methods, systems and tools for implanting long-term active therapeutic medical devices referred to as intravascular implantable devices (IID) within a patient's vasculature are disclosed. In one embodiment, the implantation techniques and instruments of the present invention are adapted for implanting an IID having only a single anchoring arrangement positioned proximate a distal portion of the device for anchoring within a vessel located superior to the heart, i.e. above the heart in a direction toward the head of a patient. Other embodiments of the invention include various methods and tools for delivering and implanting an IID, delivering and securing an anchor, and delivering and implanting one or more leads. | 2009-07-30 |
20090192580 | MEDICAL ELECTRICAL LEAD WITH BIOCOMPATIBLE LEAD BODY COATING - An intravascular medical electrical lead includes a conformal coating including at least one layer formed from a poly-p-xylylene polymer. The coating is lubricious and provides an effective barrier against moisture and gases preventing degradation of the lead body material preventing corrosion of the conductor. | 2009-07-30 |
20090192581 | ACTIVE FIXATION MEDICAL LEAD - An implantable medical device that includes an elongated body having a proximal end and a distal end, a helical fixation member extending from the distal end of the elongated body, the helical fixation member including a distal tip for affixing the distal end of the elongated body at an implant site, and a tracking member extending from the distal end of the elongated body, through the helical fixation member and outward from the distal tip of the helical fixation member for tracking along an implant pathway during implantation of the implantable medical device. | 2009-07-30 |
20090192582 | Sensor Guided Epicardial Lead - Implantable cardiac monitoring and stimulation methods and devices with epicardial leads having sensor feedback. A fixed or extendable/retractable sensor may be displaceable within the lead's lumen and configured to sense the presence of an anatomical feature or physiological parameter of cardiac tissue in proximity with the lead body's distal end. The sensor may include an ultrasonic sensing element, a perfusion sensor, a photoplethysmographic sensor, or a blood oximetry sensor. Methods of determining suitability for implanting a lead involve the steps of accessing an epicardial surface of the heart, and moving the cardiac lead to an implant site at the epicardial surface. A transmitted signal is directed at the implant site. A reflected signal is received, indicative of the presence of a blood vessel at the implant site. A determination may be made to determine whether the implant site is suitable or unsuitable based on the reflected signal. | 2009-07-30 |
20090192583 | Ordered Coatings for Drug Eluting Stents and Medical Devices - A system for treating a vascular condition comprises a therapeutic agent eluting stent having a layered coating on the stent framework. The coating releases therapeutically effective amounts of one or more therapeutic agents in and ordered sequence and over a selected time period. Another embodiment of the invention includes a method of treating a vascular condition by placing a stent having a layered coating at a treatment site and delivering a therapeutically effective amount of one or more therapeutic agents at the treatment site in an ordered sequence and over a selected time period. | 2009-07-30 |
20090192584 | Medical Systems and Related Methods - Medical systems and related methods are disclosed. In some embodiments, the medical systems include an inner tubular member defining an aperture and an outer tubular member at least partially surrounding the inner tubular member. The inner and outer tubular members can be arranged such that an implantable medical endoprosthesis can be disposed therebetween. | 2009-07-30 |
20090192585 | Delivery Systems and Methods of Implantation for Prosthetic Heart Valves - A delivery system for delivering a stented prosthetic heart valve to a lumen of a patient, the delivery system including a tubular body having a proximal end and a distal end, and a plurality of wires extending from the distal end of the tubular body, wherein each of the wires has a distal end that is coiled for engagement with a stent of a stented prosthetic heart valve. | 2009-07-30 |
20090192586 | Delivery Systems for Prosthetic Heart Valves - A delivery system for delivery of an implantable stented device to a body lumen, the device having a plurality of structures at its proximal end, wherein the delivery system comprises a first body portion removably attached to a second body portion and wherein the second body portion includes a plurality of attachment components at its distal end for attachment to the plurality of structures at the proximal end of the device. | 2009-07-30 |
20090192587 | RADIO-OPAQUE ENDOPROSTHESIS - An endoprosthesis furnished with an armature made of metal wires visible in X-ray medical imaging in which the armature is formed of at least two layers of wires, the wires forming the armature comprising a core made of a radio-opaque material, the interaction between the cores of the wires of the various layers improving the visibility of the said endoprosthesis in X-ray medical imaging. | 2009-07-30 |
20090192588 | BIODEGRADABLE DOUBLE STENT - A biodegradable double stent is used for various organs such as a biliary tract, an esophagus, an airway and a ureter. A biodegradable stent having a hollow cylindrical body woven out of a separate wire made of biodegradable polymer so as to have a plurality of rhombic spaces is fixed to an intermediate portion of a primary stent having a cylindrical body. When administered into the organ, the biodegradable stent has its original function of expanding the organ, and is firmly supported in the inner wall of a narrowed passage of the organ by pressurizing the inner wall of the narrowed passage of the organ. After a predetermined time period has elapsed, the biodegradable stent is gradually degraded away by bodily fluids, thereby enabling the primary stent to be easily removed from the organ. | 2009-07-30 |
20090192589 | INTRAVASCULAR STENT - The invention is directed to an expandable stent for implanting in a body lumen, such as a coronary artery, peripheral artery, or other body lumen. The invention provides for an intravascular stent having a plurality of cylindrical rings connected by undulating links. The stent has a high degree of flexibility in the longitudinal direction, yet has adequate vessel wall coverage and radial strength sufficient to hold open an artery or other body lumen. The stent can be compressed or crimped onto a catheter to a very low profile since the peaks that are adjacent the curved portion of the undulating link are shorter than other peaks in the same cylindrical ring to prevent overlap yet still achieve a very low profile, tightly crimped stent onto a catheter. | 2009-07-30 |
20090192590 | EXPANDABLE STENT AND METHOD FOR DELIVERY OF SAME - An expandable stent comprising a proximal end and a distal end in communication with one another and a tubular wall disposed between the proximal end and the distal end. The tubular wall has a longitudinal axis and a porous surface defined by a plurality of intersecting members comprising a series of longitudinal struts disposed substantially parallel to the longitudinal axis of the stent. Each longitudinal strut in the series comprises flexure means for substantially complementary extension and compression of a diametrically opposed pair of the longitudinal struts upon flexure of the stent. The stent is expandable from a first, contracted position to a second, expanded position upon the application of a radially outward force on the stent. The provision of such flexure means in the series of longitudinal struts leads to a very desirable balance of lateral flexibility of the unexpanded stent and radial rigidity of the expanded stent. | 2009-07-30 |
20090192591 | Markers for Prosthetic Heart Valves - A replacement prosthetic heart valve for engagement with a structure of an original prosthetic heart valve that includes at least one visually detectable marker. The replacement heart valve includes a stent structure having a generally tubular body portion and at least one visually detectable marker on a portion of the stent structure, and at least two leaflets attached within the interior area of the tubular body portion of the stent structure. At least one visually detectable marker of the stent structure is alignable with at least one visually detectable marker of the original prosthetic heart valve. | 2009-07-30 |
20090192592 | POROUS IMPLANT STRUCTURE - Exemplary embodiments of the present invention relate to an implant, e.g., a stent, and in particular to a stent having at least one section made of a material having a particular porous structure. | 2009-07-30 |
20090192593 | Stent for Delivery a Therapeutic Agent from a Side Surface of a Stent StSrut - Described herein are implantable medical devices, such as implantable or intravascular stents, for delivering a therapeutic agent, and methods for making such medical devices. In one embodiment, the medical device comprises a stent having a plurality of struts, at least one of which has a cavity disposed therein. A therapeutic agent is delivered from the cavity through and opening in a strut surface. In another embodiment, the medical device is a stent having a coating disposed on the side surface(s) of at least one strut for deliver of a therapeutic agent from the coating. | 2009-07-30 |
20090192594 | IMPLANT HAVING A BASE BODY OF A BIOCORRODIBLE ALLOY AND A CORROSION-INHIBITING COATING - An implant having a base body consisting entirely or in part of a biocorrodible metallic material wherein at least the parts of the base body made of the biocorrodible metallic material are covered with a corrosion-inhibiting coating. The coating comprises a primer layer of a first biodegradable polymer material comprising a poly(D,L-lactide) (PDLLA) with a degree of polymerization in the range of 5 to 20 and a protective layer of a second biodegradable polymer material comprising a diblock copolymer (PEG/PLGA) of polyethylene glycol (PEG) and poly(D,L-lactide-co-glycolide) (PLGA) applied to the primer layer. | 2009-07-30 |
20090192595 | MEDICAL IMPLANT - Disclosed herein is a medical implant including an implant body of which at least a part is comprised of a biodegradable metal, wherein the part comprised of the biodegradable metal has a crystal grain diameter of not more than 10 μm. | 2009-07-30 |
20090192596 | IMPLANT HAVING A BASE BODY OF A BIOCORRODIBLE ALLOY - An implant having a base body comprised entirely or partially of a biocorrodible metallic material and in which at least the parts of the base body comprising the biocorrodible metallic material are covered entirely or partially with a coating which contains or is comprised of the polymer. At least 90% of the total number of polymer units of the polymer comprise polymer units of formula (1) and polymer units of formula (2) | 2009-07-30 |
20090192597 | Surgical implant, method for the production and use thereof - A surgical implant is made from biocompatible fiber material as a woven textile fabric, in particular in the form of a vascular prosthesis, the woven fabric being so configured that its permeability to blood is so low that the blood impregnates the textile fabric upon implantation and seals it off by coagulating, but does not flow through it. | 2009-07-30 |
20090192598 | Treatment for a patient with congestive heart failure - The invention is directed to two minimally invasive therapeutic procedures, particularly for patients with congestive heart failure, and devices and systems for such procedures. One procedure involves providing a valved passageway through the patient's left ventricular wall at the apex of the patient's heart and advancing instruments through the valved passageway to connect the valve leaflets of the patient's heart valve, e.g. the mitral valve, in a “Bow-Tie” configuration to prevent or minimize regurgitation through the valve. The second procedure involves advancing a pacing lead and a pacing lead implanting device through a trocar in the patient's chest and implanting the pacing lead on an exposed epicardial region of the patient's heart wall. The pacing lead has a penetrating electrode which is secured within the heart wall. One or both procedures may be performed on a patient with CHF. | 2009-07-30 |
20090192599 | TWO-PIECE PROSTHETIC VALVES WITH SNAP-IN CONNECTION AND METHODS FOR USE - A prosthetic heart valve assembly includes a gasket member and a valve member including a plurality of fasteners and a plurality of engagement members corresponding to the fasteners. The fasteners and/or engagement members may be configured to guide the engagement members into engagement with the fasteners. For example, the fasteners may include U-shaped spring-biased clips, e.g., attached to a core or other portion of a sewing cuff of the gasket member, and the engagement members may include latches or barbed protrusions that engage one or more holes in the fasteners. During use, the gasket member is introduced into a tissue annulus, and secured to the annulus, e.g., using a plurality of clips directed through the sewing cuff. The valve member is then introduced into the annulus and the engagement members are snapped or otherwise guided into engagement with the fasteners to secure the valve member relative to the gasket member. | 2009-07-30 |
20090192600 | Sizing device having two sizers and methods of use - A sizing device for measuring a valve annulus, said sizing device comprising: an elongate segment having first and second ends; a first sizer attached to the first end of the elongate segment; and a second sizer attached to the second end of the elongate segment, wherein the first and second sizers have different shapes that correspond to the same size of valve annulus. A method of measuring a valve annulus of a heart. A system for measuring a valve annulus of a heart. | 2009-07-30 |
20090192601 | Infundibular Reducer Device Delivery System and Related Methods - Described is a delivery system for minimally invasive delivery of a self-expandable stent to a body lumen, and particularly delivery of a prosthetic valve to the right ventricular outflow tract. Also described is a method of loading a stent onto such a delivery system, and a method of delivering a self-expandable stent to a desired anatomic site. | 2009-07-30 |
20090192602 | Deformable Sizer and Holder Devices for Minimally Invasive Cardiac Surgery - Described is a device for sizing a heart valve annulus by a minimally invasive route, the device comprising: a sizing plate having first and second major surfaces, wherein the sizing plate comprises a deformable material such that the sizing plate can deform and fit through the minimally invasive route; and an elongate handle to which the sizing plate is attached. Also described is a similarly deformable device for holding an annuloplasty device. Additionally, methods of using the deformable sizing and holding devices are disclosed. | 2009-07-30 |
20090192603 | Adjustable Sizer Devices for Minimally Invasive Cardiac Surgery - Described is an adjustable device for sizing a heart valve annulus by a minimally invasive route, the device comprising: a cannula comprising a proximal end, a distal end and an interior lumen; and at least one wire extending through the interior lumen of the cannula, wherein the at least one wire may be advanced or retracted through the lumen and from the distal end of the cannula, such that a segment of the wire may form a plurality of different predetermined shapes of predetermined sizes used to size the heart valve annulus. Additionally, methods of using such adjustable sizing devices are disclosed. | 2009-07-30 |
20090192604 | Sizer, Holder and Delivery Devices for Minimally Invasive Cardiac Surgery - Described is a device for delivering a valve annulus sizer or annuloplasty device holder to a heart valve annulus, the device comprising: an elongate shaft comprising a proximal end, a distal end and at least a portion of the shaft being malleable, wherein the distal end of the elongate shaft connects to the sizer or holder. Also described are a sizer device for sizing a heart valve annulus, and a delivery device that releasably attaches a sizer device or a holder device for delivery to and/or from a heart valve annulus. | 2009-07-30 |
20090192605 | Sizer Device Having a Plurality of Anterior-Posterior Ratios - Described is a device for evaluating a heart valve annulus in order to choose a particular annuloplasty device to be attached to the annulus, wherein the annuloplasty device has an inter-trigonal or inter-commissural distance and an anterior-posterior ratio, the device comprising: a valve sizing element having one of a plurality of inter-trigonal or inter-commissural distances and comprising a plurality of indicia on the valve sizing element corresponding to a plurality of anterior-posterior ratios and used to compare to the annulus in order to indicate an anterior-posterior ratio of the annulus. Adjustable devices for evaluating a plurality of anterior-posterior ratios are also described. Also, methods of sizing a patient's heart valve annulus are described. | 2009-07-30 |
20090192606 | Holder Devices for Annuloplasty Devices Having a Plurality of Anterior-Posterior Ratios - Described is an adjustable annuloplasty device holder possible of having a plurality of different anterior-posterior ratios, the holder comprising a member having an anterior segment and a posterior segment that are shaped to hold an anterior portion and a posterior portion, respectively, of an annuloplasty device, wherein the anterior segment has a given size and the posterior segment is adjustable in order to change the anterior-posterior ratio of the holder to accommodate annuloplasty devices having a plurality of different anterior-posterior ratios. Also described is a method of using such an adjustable annuloplasty holder device. | 2009-07-30 |
20090192607 | ONE-PIECE HEART PROSTHESIS IMPLANTABLE IN AN ANATOMICAL POSITION - One-piece heart prosthesis implantable in an anatomical position. According to the invention, the artificial left and right ventricles ( | 2009-07-30 |
20090192608 | Method & apparatus for arthroscopic biceps tenodesis - A method and apparatus for arthroscopic biceps tenodesis wherein the method involves arthroscopically determining that biceps tenodesis is desirable; arthroscopically separating the long head of the biceps tendon from bone attachment; creating and placing a wedge at the proximal end of the long head of the biceps tendon; and allowing the tendon to slide through the glenohumeral joint and the wedge structure to be wedged in the bicipital groove and wherein the apparatus includes a clamshell type, button wedge having a football shaped body with top and bottom portions hinged at one end and with locking structure at an opposite end to lock the top and bottom portions together, such that staggered ribs on the top portion and bottom portion grip top and bottom surfaces of the long head of the tendon when the top and bottom portions of the button wedge are clamped together. | 2009-07-30 |
20090192609 | IMPLANT DEVICE FOR USE IN AN IMPLANT SYSTEM - An implant device | 2009-07-30 |
20090192610 | ORTHOPEDIC COMPONENT OF LOW STIFFNESS - An orthopedic component having multiple layers that are selected to provide an overall modulus that is substantially lower than the modulus of known orthopedic components to more closely approximate the modulus of the bone into which the orthopedic component is implanted. In one exemplary embodiment, the orthopedic component is an acetabular shell. For example, the acetabular shell may include an outer layer configured for securement to the natural acetabulum of a patient and an inner layer configured to receive an acetabular liner. The head of a femoral prosthesis articulates against the acetabular liner to replicate the function of a natural hip joint. Alternatively, the inner layer of the acetabular shell may act as an integral acetabular liner against which the head of the femoral prosthesis articulates. | 2009-07-30 |
20090192611 | Vertebral body replacement implant and instrument for handling the vertebral body replacement implant - In a vertebral body replacement implant having a bottom locating part for positioning against a lower vertebral body and having a top locating part for positioning against an upper vertebral body, wherein both locating parts are telescopically displaceable relative to one another in the manner of a piston-cylinder unit, having a sealed hydraulic chamber formed by the locating parts, having a charging opening leading into the hydraulic chamber for a hydraulic medium, which upon entering the hydraulic chamber pushes the two locating parts apart from one another, and having a locking device, which may be activated by means of an instrument and upon activation fixes the two locating parts non-displaceably relative to one another, in order to facilitate the handling of the vertebral body replacement implant it is proposed that the locking device is disposed on the vertebral body replacement implant in the region of the charging opening. An instrument for handling the vertebral body replacement implant is also proposed. | 2009-07-30 |
20090192612 | Vertebral body replacement implant - In a vertebral body replacement implant having a bottom locating part for positioning against a lower vertebral body and having a top locating part for positioning against an upper vertebral body, wherein both locating parts are steplessly displaceable relative to one another along a displacement path so that the height of the vertebral body replacement implant is variable, having a clamping device for fixing the two locating parts in any desired intermediate position along the displacement path, which clamping device comprises a clamping element that is mounted on one locating part so as to be variable in position and can be pressed towards a clamping face on the other locating part, in order to improve the clamping action it is proposed that the clamping face is inclined slightly relative to the displacement path, so that when the locating parts are pushed together the clamping face moves progressively closer to the clamping element. | 2009-07-30 |
20090192613 | STANDALONE DYNAMIC INTERBODY - An intervertebral implant includes a first plate and a second plate that is configured to be moveably engaged with the first plate along an axis of translation. Each plate defines at least one hole or recess for receiving a fastener that is configured to be fastened to a respective vertebrae. In one embodiment, a toothed surface is defined on both the first plate and the second plate. The toothed surface of the first plate is configured for engaging the toothed surface of the second plate such that translation of the second plate with respect to the first plate is limited in a single direction along the axis of translation. | 2009-07-30 |
20090192614 | Intervertebral implant - In order, in an intervertebral implant having a core made of a swellable material and having a vertebral-body locating face on its top and/or bottom side, which is connected to the swellable core, to reduce the shearing forces between the swellable core and the vertebral-body locating face during swelling of the swellable core, it is proposed that the vertebral-body locating face comprises a plurality of support elements, which are respectively anchored adjacent to one another and individually in the core, and a plurality of mutually separate locating elements, which are disposed adjacent to one another and outside of the core and which are carried by the support elements and are movable relative to one another in the plane of the vertebral-body locating face. | 2009-07-30 |
20090192615 | HYDROSTATIC INTERBODY - An intervertebral implant includes an upper surface configured for engagement with a first vertebral body, and a lower surface configured for engagement with a second vertebral body. A wall extends between the upper surface and the lower surface, and forms a chamber for containing osteogenic material. At least a portion of the wall is collapsible from a first position associated with a first volume of the chamber to a second position associated with a second volume of the chamber. The second volume is less than the first volume. | 2009-07-30 |
20090192616 | ARTIFICIAL SPINAL DISK - An artificial spinal implant for placement between adjacent vertebrae to replace disk material and to stabilize the involved vertebrae is described. The artificial disk may be disassembled for installation and/or removal for repair, replacement or adjustment, and may be assembled from the front of the spine as individual component parts, thereby permitting alignment of the spine during the assembly process, and the stabilization of the involved vertebrae once assembly has been completed. Further, the components may be chosen from a set of similar components having different sizes, thereby enabling the implant to be tailor fit to the requirements of the patient. | 2009-07-30 |
20090192617 | Intervertebral Prosthetic Disc With Shock Absorbing Core Formed With Disc Springs - An artificial intervertebral disc has upper and lower prosthesis plates disposed about a shock absorbing mobile core. The shock absorbing core includes one or more spring washers or disc springs between rigid upper and lower surfaces of the core to allow the upper and lower surfaces to move resiliently toward and away from each other. This allows the core to absorb forces applied to it by the vertebrae. The components of the shock absorbing core including the disc springs are formed of rigid materials having high durability and biocompatibility. | 2009-07-30 |
20090192618 | ARTIFICIAL SPINAL DISK - An artificial spinal implant for placement between adjacent vertebrae to replace disk material and to stabilize the involved vertebrae is described. The artificial disk may be disassembled for installation and/or removal for repair, replacement or adjustment, and may be assembled from the front of the spine as individual component parts, thereby permitting alignment of the spine during the assembly process, and the stabilization of the involved vertebrae once assembly has been completed. Further, the components may be chosen from a set of similar components having different sizes, thereby enabling the implant to be tailor fit to the requirements of the patient. | 2009-07-30 |
20090192619 | Passive electro-magnetically damped joint - The present invention comprises an apparatus, system and method utilizing a passive electro-magnetically damped joint for prosthetics or orthotics. Such as system may be controlled through changing the resistive nature of the circuit in which a braking or damping mechanism can sufficiently replicate and augment biomechanical movement. This may be accomplished through electronic circuitry means only, or through the use of intelligent control through a microprocessor and dynamic ambulation replication algorithms. | 2009-07-30 |
20090192620 | PROSTHETIC DEVICE AND METHOD FOR IMPLANTING THE PROSTHETIC DEVICE - A substantially cup-shaped prosthetic device for a joint is provided. The prosthetic device includes an outer surface configured to operatively engage at least one of a first bone of the joint and a component, an inner surface including at least a portion configured to connect to a second bone of the joint, and at least one reservoir having an opening at each of the inner surface and the outer surface and extending therebetween. | 2009-07-30 |
20090192621 | Shoulder Implant Assembly - An implant assembly and associated method for selectively performing reverse and traditional arthroplasty for a shoulder joint that includes a humerus and a glenoid. The implant assembly may include a head, a cup, a humeral stem and an adaptor. The method includes inserting the humeral stem to the humerus and connecting a male taper of the adaptor to a female taper of the head. For reverse arthroplasty, the method includes attaching the adaptor to the glenoid and the cup to the stem. For traditional arthroplasty, the method includes attaching the adaptor to the humeral stem and the cup to the glenoid. The method also includes articulating the head with the cup. | 2009-07-30 |
20090192622 | Extended Articulation Orthopaedic Implant - A prosthesis ( | 2009-07-30 |
20090192623 | MODULAR HUMERAL HEAD - A modular humeral head system includes a housing having an outer surface and an inner surface. A hemispherical socket formed on one end of the inner surface and threads formed on the other end of the inner surface. A cap is attached at the threaded end of the housing. The cap has one or more threaded holes that run from the top surface to bottom surface of the cap. A screw may be inserted in each hole. The modular humeral head system also includes an intermediate piece having a hemispherical head at one end of a tapered shaft. The tapered shaft is inserted in a humeral stem. The hemispherical head and the hemispherical socket form a ball and socket coupling. A trial head may be impacted on the housing. The trial head has one or more holes that are aligned with the screws inserted in the cap. | 2009-07-30 |