Abstract: A surgical inserter for use in inserting an implant into a vertebral space may include: (a) a handle; (b) a gripper having one end attached to the handle and a second end having a pair of arms; and (c) a grip activator having an opening that threadingly receives the gripper. The grip activator can be rotated in a first direction with respect to the gripper to cause the arms to move toward each other to grip the inserter and in a second direction with respect to the gripper to cause the arms to move away from each other to release the inserter. In one embodiment a compression force activator is used to deploy the implant and in another embodiment a tension force activator is used to deploy the implant.

Abstract: A spinal implant is provided for retaining spinal elements in a desired spatial relationship. It includes a tensioning member positionable along the spinal column of a patient to match the contour thereof. A pair of buttress members are located each on one of the ends of the tensioning member, at least one of the buttress members being slidable on the tensioning member so that the distance between the buttress members may be adjusted.

Abstract: A bifurcated intravascular stent graft comprises primary stent segments and a primary graft sleeve, forming a main fluid channel and having a side opening therethrough. An external graft channel formed on the primary graft sleeve has a first end communicating with the side opening and an open second end outside the primary graft sleeve, thereby providing a branch flow channel from the main channel out through the side opening and external graft channel. The primary stent segments and graft sleeve engage an endoluminal surface of a main vessel and form substantially fluid-tight seals. The stent graft further comprises a secondary stent graft, which may be positioned partially within the external graft channel, through the open second end thereof, and partially within a branch vessel. The secondary stent graft engages the inner surface of the external graft channel and the endoluminal surface of the branch vessel, thereby forming substantially fluid-tight seals.

Abstract: Instrumentation for implanting an artificial intervertebral disc includes static trials and a dynamic trial for determining the appropriate size of disc to be implanted, static trial holders for manipulating the static trials, inserter/impactors for inserting and removing the static trials and for inserting the artificial intervertebral discs, repositioners/extractors for repositioning and extracting the static trials or the artificial intervertebral discs, and a leveler for setting the proper position of the artificial intervertebral disc. Methods for using the same are also disclosed. Features for artificial intervertebral discs and intervertebral spacer devices useful for manipulation by the instrumentation are also disclosed.

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: A method for delivering a spinal implant into a vertebral space, including providing a spinal implant, providing a die member defining an opening sized to receive the implant while in an initial configuration, inserting the implant into the opening in the die member, displacing the implant relative to the die member, transitioning the implant from the initial configuration to a deformed configuration having a reduced lateral profile relative to the initial configuration, and discharging the implant from the die member and inserting the implant into the vertebral space while in the deformed configuration.

Abstract: Orthopaedic implants, orthopaedic implant sets, and/or methods for making the same. Aspects and embodiments of the present invention may include orthopaedic implants having an elongated insertion region including proximal, distal, and transition portions, wherein at least portions of at least one face each of the proximal and transition portions are defined by spaced apart constant radii of curvature. The same or other aspects and embodiments may include sets of orthopaedic implants in which proximal portions of the implants grow at different rates than distal portions of the implants. The same or other aspects and embodiments may include methods for making implants and/or sets of implants by studying the geometries of differently sized bony anatomies.

Abstract: An insertion system for release of a self-expanding stent device 18 in a body vessel has a first grip 33, which is fixedly connected to a shaft 15, a second grip 36, which is mounted on the shaft 15 to be movable in axial direction, a sheath 19, which, in a distal portion thereof, keeps the stent device radially compressed and which is fixedly connected to the second grip 36, and a retention element 17, which is fixedly connected to the shaft 15 and is guided in the sheath 19, wherein the retention element 17 holds the stent device 18 in its axial position relative to the first grip 33 when the sheath 19 is being retracted. Reference means 25 with an optical reference mark 26 are arranged for continuous monitoring of the axial position of the stent device 18.

Abstract: A spinal implant comprising a hollow body having a leading end, a trailing end and a pair of lateral walls extending from the leading end to the trailing end, the lateral walls including concave, non-threaded inner surfaces defining an internal space of the hollow body. The implant includes an anchoring member insertible between the lateral walls and into the internal space of the hollow body, the anchoring member having bone anchoring projections defining an outer diameter of the anchoring member. When the anchoring member is inserted into the internal space of the hollow body, the concave inner surfaces of the lateral walls substantially conform to the outer diameter of the anchoring member.

Abstract: A guide that facilitates the creation of two bone tunnels for use during a “double bundle” cruciate ligament repair. In the case of an anterior cruciate ligament repair the guide facilitates the formation of two tibial tunnels extending between a single aperture on the anterior tibia and two distinct apertures on the tibial plateau. The guide has a single angled throughbore for guiding a drill bit on a predetermined angle relative to the anterior portion of the tibial tunnel. In an alternative embodiment the guide has two independent and non-intersecting bores which allow the simultaneous placement into the tibial tunnel of two separate guide pins to guide the formation of two tibial tunnels on the tibial plateau.

Abstract: A delivery device for positioning and deploying an implantable device within a lumen is provided. The delivery device includes inner and outer tubular members slidable to each other between at least a first hold position and a second release position, a handle and a deployment mechanism adapted for an operator to use a first hand for operating the delivery device and moving the tubular members between the first and second positions. The delivery device further includes a protective member adapted for insulating at least a portion of the outer tubular member from the tendency of the operator to use his or her second hand to grab the outer tubular member during operations or from other external forces.

Abstract: Medical devices, such as endoprostheses, are disclosed. In some embodiments, an endoprosthesis includes a circumferentially-oriented band including two curved portions and a first portion connecting the two curved portions, the first portion having a first width and at least one curved portion having a second width; and a connector extending from the band; wherein the second width is greater than the first width.

Abstract: A heart valve assembly includes a base including a multi-lobular annular shape within a plane, a valve member or other annular body including a multi-lobular shape complementary to the shape of the base, and cooperating connectors on the base and the annular body for connecting the annular body to the base. The base includes an anchoring ring, and a flexible cuff for attaching the base to a biological annulus. The base and the annular body include guides for aligning their multi-lobular shapes, e.g., visual, tactile, or other markers, or tethers that extend from the base that are slidable through the annular body. During use, the base is attached to a biological annulus, the annular body is directed adjacent the annulus, oriented such that the multi-lobular shape of the annular body valve member is aligned with the base, and the annular body is attached to the base.

Abstract: Instrumentation for implanting an artificial intervertebral disc includes static trials, the static trials including first and second trial baseplates immovably coupled to one another via a trunk extending therebetween, each trial baseplate having an outwardly facing surface approximating a contour of a corresponding outwardly facing surface of an artificial intervertebral disc baseplate, at least one of the trial baseplates having a plurality of engagement holes extending into the at least one of the trial baseplates in a direction substantially perpendicular to each of a plurality of a surgical approach directions used to insert the trial into the intervertebral space, each of the plurality of engagement holes being disposed on the at least one of the trial baseplates to correspond to a respective one of the surgical approach directions such that selection for use of one of the plurality of engagement holes corresponds to, selection of the respective surgical approach.

Abstract: An injectable material delivery device is disclosed and can include a barrel that can have an internal chamber. A plunger can be at least partially disposed within the internal chamber of the barrel. Further, a collapsible mixing blade can be disposed within the internal chamber.

Abstract: A recess-ramp knee joint prosthesis comprising a femoral and a tibial component is configured to reproduce normal kinematics and function. Asymmetric condular surfaces and a cupola of the femoral component interact with corresponding dished surfaces and a ramp of the tibia thereby duplicating the behavior of the anatomical knee.

Abstract: An apparatus, system, and method are disclosed for positional fixation of a fastener, including but not limited to the extraction of an orthopedic screw. According to one embodiment, an instrument is provided which accepts a collet designed to conform to a proximal end of a variety of types and sizes of fasteners. The collet is installed through a chuck body, which is seated in a distal end of a handle. A closing mechanism within the handle causes the collet to tightly grip and lock onto the proximal end of the fastener. A compressible distal end of the collet may have longitudinal slits that define jaws for improving gripping flexibility.

Abstract: A vascular repair device includes a tubular graft body and a structural framework having at least two stents connected to the graft body. Stents of the structural framework can each be respectively connected to graft body adjacent the proximal and ends and the support member is shorter than the separation distance therebetween to form a gimbal at least at one end. A first stent is connected along an entirety thereof and a second stent is connected at distal apices thereof. Distal apices of the second stent have radii of curvature smaller than proximal apices. A curved longitudinal support member can be connected to the graft body, the support member being substantially symmetrical with respect to the centerline. The support member can be connected to the graft body independent of the structural framework. At least one of the ends of the support member can have a curved longitudinal extremity.

Abstract: Novel ergonomically designed hand held surgical tissue Z-shaped retractors. The retractors include retractor plates which are angulated and deviated from the main axis along the handle of the retractor. The retractors may be applicable for general, cosmetic and reconstructive surgeries, cardio, vascular, obstetrics/gynecology applications, and veterinary practices.

Abstract: A stent combined with a positioning apparatus to effectively place the stent at a precise deployment site within a narrowed vascular region such as an artery. The stent is maneuvered through the vessel and is guided by a guiding catheter up the vessel to where the narrowing is located. Upon exiting the guiding catheter and approaching the deployment site within the coronary artery, a deployment site locator expands to contact the vascular structure and, thereby, effectively position the stent at the deployment site within the narrowed vessel. This system apparatus and method is particularly useful for stent placement at an ostium (origin) of a vessel.