Abstract: The disclosure of the invention provides an implantable structural element for in vivo delivery of bioactive agents to a situs in a body. The implantable structural element may be configured as an implantable prosthesis, such as an endoluminal stent, cardiac valve, osteal implant or the like, which serves a dual function of being prosthetic and a carrier for a bioactive agent. Alternatively, the implantable structural element may simply be an implantable article that serves the single function of acting as a time-release carrier for the bioactive agent.

Abstract: An apparatus for implantation in an annulus of a tricuspid valve. The apparatus has an anterior annulus aspect, a posterior annulus aspect, and an atrioventricular (AV) node located adjacent the anterior annulus aspect. The apparatus includes an ovoid main body portion. The main body portion has an anterior body segment adapted for placement adjacent the anterior annulus aspect, a posterior body segment located opposite the anterior body portion and adapted for placement adjacent the posterior annulus aspect, and oppositely disposed left and right side body segments extending between the anterior and posterior body segments. At least two valve leaflets are secured within the main body portion and are coaptable to permit unidirectional flow of blood. A cushioned section is attached to the main body portion, coextends with a portion of the main body portion, and is adapted for placement adjacent the AV node.

Abstract: A method of positioning a main stent at a vessel bifurcation includes positioning a main guidewire in the main vessel; and advancing a stent delivery system to a position proximate the bifurcation. The stent delivery system includes a catheter with a flexible side sheath attached thereto and a main stent positioned over the catheter. The flexible side sheath is positioned to pass through the side opening in the main stent. The method also includes advancing a branch guidewire through the flexible side sheath and into the branch vessel; and subsequently, advancing the catheter over the main guidewire while advancing the flexible side sheath over the branch guidewire while viewing relative movement of a marker positioned on the flexible side sheath with respect to at least one marker positioned on the catheter.

Abstract: Expandable, percutaneously deployable, prosthetic heart valves and systems for minimally invasive replacement of damaged or diseased native aortic valves comprise an expandable, tubular stent body and a unidirectional valve assembly. Embodiments of the stent body comprise an annulus anchoring section, a sinus section, and an outflow section, with the outflow section flared outward from the sinus section in an expanded configuration. Embodiments of the stent body are self-expanding, comprising, for example nitinol. The valve assembly disposed within the sinus section of the stent body and sutured thereto. Embodiments of the valve assembly comprise three leaflets, each leaflet comprising a curved outer edge sutured to the sinus section of the stent body, and a coapting free edge. Embodiments of the valve leaflets comprise pericardium. Embodiments of the prosthetic heart valve have a contracted configuration dimensioned for percutaneous delivery thereof.

Abstract: A femoral head surgical resurfacing aid that includes a C-shaped band with an interior surface conformed to fit a femoral neck of a patient is presented. An arch extends from one side of the C-shaped band to the other side of the C-shaped band and further extends over a femoral head of the patient. An alignment tube guide is positioned along the arch and extends outward from the arch.

Abstract: A spinal implant for replacing the natural nucleus of the disc made from a polymer such as hydrogel having a radiopaque material located within the polymer. The material may be in the form of a powder dispersed throughout the polymer or may be in he form of a powder dispersed in layers or in other specific locations within the polymer. The radiopaque material is metal such as gold, tungsten, titanium, tantalum or platinum. The metal may also be in the form of a foil or wire located within the hydrogel such as polyurethane, thereby making the implant visible on x-rays. Other polymers besides hydrogel may be used with the radiopaque material being dispersed therein.

Abstract: A medical device that can be used for treating a defective heart valve. One aspect of the invention pertains to a longitudinally adjustable medical device that comprises a distal portion, a proximal portion, and a cord member. The distal portion comprises a distal anchoring member, a distal telescope, and a distal backbone. The proximal portion comprises a proximal anchoring member, a proximal telescope, and a proximal backbone. The distal backbone and the proximal backbone are configured to provide a structural support to the device while providing flexibility to the device. The cord member is disposed within the device and used to facilitate longitudinal adjustment for the device.

Abstract: A soft tissue tensioning system comprises a manual suture tensioning device having a bar and a finger guard which is orthogonal to the bar. A lateral suture cleat is disposed on each lateral end of the bar, and a primary suture cleat extends about a top and a bottom of each of the opposed lateral ends of the bar.

Abstract: A stent includes a coiled-up sheet having overlapping inner and outer longitudinal sections extending parallel to a longitudinal axis thereof, and defining a periphery, the coiled-up sheet being unrollable between contracted and enlarged conditions. A plurality of stretchable elements are formed in the coiled-up sheet, the stretchable elements being expandable about the periphery between an unstretched condition to facilitate placement in a delivery device in the contracted condition and a stretched condition to facilitate expansion of the coiled-up sheet to the enlarged condition upon deployment from the delivery device. Preferably, the coiled-up sheet is biased to the enlarged condition, and the stretchable elements are biased to the stretched condition. More preferably, at least one of the biases is provided by a shape memory property of the coiled-up sheet, which is activated by exposing the stent to body temperature.

Abstract: A sinus correction method is disclosed. For example, one embodiment comprises making an incision in gingival tissue surrounding a sinus membrane perforation, dissecting the gingival tissue from cortical bone, dissecting sinus membrane adjacent to the gingival tissue from the cortical bone, overlapping the sinus membrane and adjacent gingival tissue from two sides of the sinus membrane perforation, connecting the overlapping sinus membrane and adjacent gingival tissue from two sides of the sinus membrane perforation, and applying a bone graft composition adjacent to the overlapping sinus membrane, the bone graft composition to form bone connected with cortical bone sufficient to place a dental implant.

Abstract: A method for controlling the mutual angle between the parts of an artificial hip joint during an operation for insertion of the artificial hip joint, is described. The stem of the femoral hip prosthesis is fastened permanently or removable in the usual manner in the proximal end of the femur. A tool for controlling of the mutual angle between the stem of the prosthesis and the cup of the prosthesis is fastened to the stem. The femur of the patient is then oriented in a predefined position and the cup is then brought into its intended position by means of the femur of the patient and the mentioned tool. A tool for controlling the mutual angle between the parts of the artificial hip joint is also described.

Abstract: An intervertebral prosthesis, in particular for the cervical spine, includes a first cover plate to be connected to a first vertebral body, second cover plate to be connected to the second vertebral body, and a prosthesis core which forms an articulation with the second cover plate. The prosthesis core is held by seat of the first cover plate which is designed as a guide device. The core can be pushed into the guide device from the ventral side in the anterior-posterior (AP) direction relative to the first cover plate. A limit-stop plate is provided on the ventral edge of the first cover plate. This limit-stop plate is displaceable in a slide guide between a locking position and a nonlocking position.

Abstract: A stent delivery system for implantation of a stent in a vessel includes an outer tubular member having a restraining sheath and an inner tubular member having a distal end which has a compressed stent mounted thereto. The proximal end of the inner tubular member is connected to a housing assembly which prevents the inner tubular member from moving when the outer tubular member is retracted to deploy the stent. The proximal end of the outer tubular member is attached to a pull-back handle which is slidably mounted on the base of the housing assembly. When the pull-back handle is retracted, the restraining sheath is retracted to deploy the sheath, while the inner tubular member remains stationary.

Abstract: An intervertebral spacer device includes first and second plates disposed in a spaced apart relationship, each plate having an inner surface and an outer surface, the inner surfaces of the opposing plates facing one another. The device also includes a restoring force providing element disposed between the inner surfaces of the plates. The restoring force providing element includes a slotted belleville washer having a convex shape when unloaded and a flatter shape when loaded, whereby one or more slots of the belleville washer widen when compressively loaded. The second plate has an annular groove formed in the inner surface of the second plate, the device including a retaining wall and a retaining ring, whereby a wide end of the belleville washer is captured by the retaining wall and the retaining ring for maintaining the wide end adjacent the inner surface of the second plate.

Abstract: A stent includes a central portion of helically wound undulations formed of struts, cylindrical end portions, and transition zones between the helical portion and the cylindrical portions. According to a first aspect of the invention, the torsional flexibility of the stent is maximized by having bridges connecting adjacent winding be interrupted by the maximum possible number of undulations. In a preferred design, each winding includes nineteen undulations around the circumference, bridges are provided every five undulations. According to a second aspect of the invention, uniform, opening of the transition zone is achieved by altering the width, and thereby the flexibility, of a series of struts in accordance with their lengths. Specifically, the long transition zone struts are made wider.

Abstract: Described herein is an intervertebral disk prosthesis with an angled leading edge for insertion into the Intervertebral space. The disk prosthesis may provide for both rotation and compression.

Abstract: Articulating diamond-surfaced spinal implants are disclosed. The implants use sintered polycrystalline articulation surfaces which are attached to spinal endplates and which are implanted to replace damaged spinal joints. The implants provide a long wearing and biocompatible articulation surface. Materials which may be used to make the spinal implants and manufacturing and finishing techniques for making the implants are also disclosed.

Abstract: A cervical intervertebral disk prosthesis has two cover plates, at least one of which is provided with a wedge-shaped connection surface for connection to a vertebral body and which is wider than it is deep. The dorsal edge of the connection surface may be set back from the dorsolateral edge of the cover plate having the connection surface and be connected to the dorsal edge, protruding above it, via a rounding or bevel.

Abstract: The vasoocclusive apparatus can be used in a method of interventional therapy and vascular surgery by inserting the apparatus into a portion of a vasculature, for treatment of a body vessel such as an aneurysm in conjunction with a secondary vasoocclusive device to be placed within the vessel. The vasoocclusive Vasooclusive apparatus includes a plurality of strut members connected together at a central hub that extend from a collapsed position to an expanded configuration to cross the neck of the aneurysm, dividing the neck into smaller openings, allowing the deployment of the secondary vasoocclusive device within the aneurysm but preventing migration of the secondary vasoocclusive device from the aneurysm. The strut members can be made from a twisted cable of strands of a superelastic material, such as a shape memory nickel titanium alloy, with at least one radiopaque strand.

Abstract: A method of cutting material for use in an implantable medical device employs a plotted laser cutting system. The laser cutting system is computer controlled and includes a laser combined with a motion system. The laser precisely cuts segments out of source material according to a predetermined pattern as designated by the computer. The segments are used in constructing implantable medical devices. The cutting energy of the laser is selected so that the cut edges of the segments are melted to discourage delamination or fraying, but communication of thermal energy into the segment beyond the edge is minimized to avoid damaging the segment adjacent the edge.