Abstract: Endoprosthesis, such as a stent, includes at least one annular element defined by a first set of strut members interconnected to define apices proximate opposite sides of the annular element. The annular element further includes a foot extension extending between at least one pair of circumferentially-adjacent strut members. The foot extension has first and second foot portions extending circumferentially from corresponding ends of the circumferentially-adjacent strut members, and are contoured to provide at least two areas of flexure. The first and second foot portions are joined at a toe portion of the foot extension, and define a circumferentially-directed apex between the pair of circumferentially-adjacent strut members. Preferably, at least one or more additional annular elements, each defined by interconnected strut members, are provided. The annular elements are generally expandable between a delivery configuration and a deployed configuration.

Abstract: An apparatus for replacing a damaged spinal disc in a spinal column includes a resilient core having a first surface and a second surface. A first retaining device is connected to the first surface of the resilient core. The first retaining device includes an outer surface engageable with a first vertebra of the spinal column and an inner surface facing the first surface of the resilient core. A second retaining device is connected to the second surface of the resilient core. The second retaining device has an outer surface engageable with a second vertebra of the spinal column and an inner surface facing the second surface of the resilient core. The inner surface of the first retaining device is spaced from the core. The core deflects into engagement with the inner surface of the first retaining device upon relative movement between the first and second retaining devices.

Abstract: A meniscal allograft with a bone block having a trapezoidal shape in cross-section and a technique for using a meniscus allograft having a trapezoidal shaped bone block are disclosed. A groove is formed initially in the bone using drill bits. Dilators are used to increase the size of the drilled groove. The orthogonal corner at the bottom of the groove is shaped using a rasp. A smooth dilator compacts the bone in the acute angle at the bottom of the groove opposite the orthogonal corner to create the final trapezoid shape of the bone groove. A meniscal allograft having a bone block of corresponding trapezoidal shape is prepared using a workstation and three cutting jigs to make three corresponding cuts. The trapezoidal bone block of the meniscal allograft is then installed within the bone groove.

Abstract: A breast prosthesis has an adhesive element which forms a continuous surface conforming to the back section of the prosthesis which faces the user. One side of the adhesive element is detachably secured to the back section of the prosthesis and the other side of the adhesive element is detachably adhered to the user. The adhesive element is formed from an inner body which is lined with material. The breast prosthesis has a flat annular region on its back section and an elevated edge along the perimeter of the flat annular region. A gap is provided in the elevated edge at an upper region of the prosthesis. The adhesive element extends to the inner surface of the elevated edge and has a projection conforming to the gap.

Abstract: A device for inducing weight loss in a patient includes a tubular prosthesis self-expandable from a collapsed position in which the prosthesis has a first diameter to an expanded position in which the prosthesis has a second, larger, diameter. In a method for inducing weight loss, the prosthesis is placed in the collapsed position and inserted into a stomach of a patient. The prosthesis is allowed to self-expand from the collapsed position to the expanded position and into contact with the walls of the stomach, where it induces feelings of satiety and/or inhibits modulation of satiety-controlling factors such as Ghrelin.

Abstract: A polymeric material such as polyurethane, PET, or ePTFE is used to cover an intravascular stent. The cover material has an overlapping portion which is slidable upon itself so that when the stent is expanded, the cover material does not contribute to stent foreshortening, if any. The cover material can be provided with holes to permit endothelialization and can be drug loaded to facilitate repair of a damaged vessel.

Abstract: Instruments and methods for inserting and expanding interbody spinal fusion implants having an expandable height.

Abstract: The present invention is a specialized orthopedic implant having an exterior surface for engaging bone. The surface comprises arrayed projections having at least one forward facing facet directed at least in part toward the leading end of the implant and at least one rearward portion directed at least in part toward the opposite trailing end of the implant. Each of the forward facet and rearward portion has a length and a slope. The length of the forward facet is longer than the length of the rearward facet. The slope of the rearward facet is steeper than the slope of the forward facet. The surface projections also have opposed side facets directed generally toward the sides of the implant. The side facets are located between the forward facet and rearward facet and converge toward each other in a direction away from the base of the surface projections. The surface may also include projections having left and right forward side facets and a rearward facet.

Abstract: A device for inducing weight loss in a patient includes a tubular prosthesis self-expandable from a collapsed position in which the prosthesis has a first diameter to an expanded position in which the prosthesis has a second, larger, diameter. In a method for inducing weight loss, the prosthesis is placed in the collapsed position and inserted into a stomach of a patient. The prosthesis is allowed to self-expand from the collapsed position to the expanded position and into contact with the walls of the stomach, where it induces feelings of satiety and/or inhibits modulation of satiety-controlling factors such as Ghrelin.

Abstract: An eyelid implant for implanting in an upper eyelid of a person having a main body with a water-drop shape. The main body has a head end with a center of gravity at substantially a center point thereof, and a tail end. The diameter of the head end is greater than a diameter of the tail end. At least one suture hole extends completely through the main body. At least one suture channel extends partially through the main body to a predetermined depth. A suture is passed through the at least one suture hole for securing the eyelid implant to an eyelid of a user and said implant causes said eyelid to close.

Abstract: An expandable intraluminal endoprosthesis including a tubular member (1) a first diameter which permits intraluminal delivery of the member into a lumen of a body passageway, particularly a blood vessel. The tubular member (1) is capable of acquiring a second, expanded and deformed diameter upon the application from the interior of the tubular member of a radially outwardly extending force, which second diameter is variable and dependent on the amount of the force applied to the tubular member. Such a tubular member may be expanded and deformed to expand the lumen of the body passageway. The wall of the tubular member includes a substantially continuous structure (2) of mutually staggered undulations. This structure has been separated from a tube wall and exhibits at least one pattern which advances substantially helically along a longitudinal axis of the tubular member. Connection elements within the structure connect adjacent undulations to each other.

Abstract: In a joint prosthesis with a base piece for anchoring in the bone, a collar piece articulated thereon and defining a collar axis, and a collar extension on the collar piece situated on the collar axis, an articulation space is formed on the base piece. An articulation head of the collar piece is disposed therein. The joint prosthesis further includes a head cap disposed on the collar extension and at least one pressure piece for pressing the articulation head against the base of the articulation space. The pressure piece and the base piece can be connected. In a joint prosthesis of this kind, the pressure piece includes a pressure disc with a passage opening for the collar extension.

Abstract: Devices, systems, and methods are provided for accessing the interior of the heart and performing procedures therein while the heart is beating. In one embodiment, a tubular access device having an inner lumen is provided for positioning through a penetration in a muscular wall of the heart, the access device having a means for sealing within the penetration to inhibit leakage of blood through the penetration. The sealing means may comprise a balloon or flange on the access device, or a suture placed in the heart wall to gather the heart tissue against the access device. An obturator is removably positionable in the inner lumen of the access device, the obturator having a cutting means at its distal end for penetrating the muscular wall of the heart. The access device is preferably positioned through an intercostal space and through the muscular wall of the heart.

Abstract: This invention relates to a spinal facet joint ligament.

Abstract: The present invention comprises an artificial disc for a spine and methods of implanting the same. The artificial disc includes an upper and lower endplate to be coupled to upper and lower vertebral bodies. A core of shaped memory alloy material is placed between the endplates to mimic the spinal disc.

Abstract: A ventilation tube has a tubular member with generally circular flanges at opposite ends. Each flange has a respective tab that is angled obliquely to the axis of the tubular member. The tabs are diametrically opposite, and angled in opposite senses. Each tab has straight non-cutting edges tangential to its associated flange, and an arcuate nose portion. Each flange (may be used either for grasping the ventilation tube, or for insertion into an incision in a tympanic membrane, thereby permitting the ventilation tube to be used reversibly.

Abstract: The present invention generally comprises a fixed bearing prosthesis and a mobile bearing prosthesis. The fixed bearing prosthesis comprises a tibial component, a femoral component and a meniscal component and addressees the loss of congruency during deep knee flexion and the possible direct, repetitive contact of the tibial and femoral components. The tibial component of the fixed bearing prosthesis includes a tibial platform having an anterior and posterior edge. The meniscal component of the fixed bearing prosthesis includes a posterior ridge overlapping the posterior edge of the tibial platform that prevents metal-to-metal contact during deep knee flexion. The mobile bearing prosthesis comprises generally a tibial component, a femoral component and a meniscal component addresses the lack of conformity to natural biomechanical movement.

Abstract: A joint and method for producing a joint in an endovascular graft. In one embodiment, a flap of a flexible material portion of an endovascular graft is folded about a portion of an expandable member to form a loop portion. The flap is secured in the loop configuration so that tensile force on the expandable member is transferred into a shear force on the fixed portion of the flap.

Abstract: A porous weave of bioabsorbable filaments having an open mesh configuration is formed into an oblate shape having dimensions greater than the esophageal opening and gastric outlet of a stomach. The resulting prosthesis is deployed in the stomach and is of a size to be retained in the proximate portion thereof for exerting pressure on the upper fundus. The prosthesis limits the amount of food that may be held within the stomach, and exerts pressure on the fundus to create a sensation of being full, resulting in weight loss.

Abstract: A method for treatment of mitral annulus dilatation comprises reducing the circumference of the mitral valve annulus. The method further comprises inserting an elongate body into the coronary sinus in the vicinity of the posterior leaflet of the mitral valve, fixing the position of the elongate body relative to the coronary sinus, and changing the shape of the elongate body in order to remodel the mitral valve annulus.