Abstract: A repaired tendon includes a proximal tendon section having a free end, and a distal tendon section having a free end that opposes the free end of the proximal tendon section. Four bidirectional barbed sutures are implanted in the repaired tendon for approximating the free end of the proximal tendon section with the free end of the distal tendon section. Each of the four bidirectional barbed sutures includes a proximal section having proximal barbs that engage the proximal tendon section, a distal section having distal barbs that engage the distal tendon section, and a stop located between the proximal and distal barbs that engages the approximated free ends of the proximal and distal tendon sections. The bidirectional barbed sutures have first suture bites and second suture bites that are shorter than the first suture bites.

Abstract: A repaired tendon includes a proximal tendon section having a free end, and a distal tendon section having a free end that opposes the free end of the proximal tendon section. Four bidirectional barbed sutures are implanted in the repaired tendon for approximating the free end of the proximal tendon section with the free end of the distal tendon section. Each of the four bidirectional barbed sutures includes a proximal section having proximal barbs that engage the proximal tendon section, a distal section having distal barbs that engage the distal tendon section, and a stop located between the proximal and distal barbs that engages the approximated free ends of the proximal and distal tendon sections. The bidirectional barbed sutures have first suture bites and second suture bites that are shorter than the first suture bites.

Abstract: The present invention relates to tissue-supporting medical devices and drug delivery systems, and more particularly to tubular flexible stents that are implanted within a body lumen of a living animal or human to support the organ, maintain patency and/or deliver drugs or agents. The tubular flexible stent has a cylindrical shape defining a longitudinal axis and includes a helical section having of a plurality of longitudinally oriented strut members and a plurality of circumferentially oriented hinge members connecting circumferentially adjacent strut members to form a band. The band is wrapped about the longitudinal axis in a substantially helical manner to form a plurality of helical windings. At least one connector member extends between longitudinally adjacent helical windings of the band.

Abstract: The present invention relates to tissue-supporting medical devices and drug delivery systems, and more particularly to tubular flexible stents that are implanted within a body lumen of a living animal or human to support the organ, maintain patency and/or deliver drugs or agents. The tubular flexible stent has a cylindrical shape defining a longitudinal axis and includes a helical section having of a plurality of longitudinally oriented strut members and a plurality of circumferentially oriented hinge members connecting circumferentially adjacent strut members to form a band. The band is wrapped about the longitudinal axis in a substantially helical manner to form a plurality of helical windings. At least one connector member extends between longitudinally adjacent helical windings of the band.

Abstract: The present invention relates to tissue-supporting medical devices and drug delivery systems, and more particularly to tubular flexible stents that are implanted within a body lumen of a living animal or human to support the organ, maintain patency and/or deliver drugs or agents. The tubular flexible stent has a cylindrical shape defining a longitudinal axis and includes a helical section having of a plurality of longitudinally oriented strut members and a plurality of circumferentially oriented hinge members connecting circumferentially adjacent strut members to form a band. The band is wrapped about the longitudinal axis in a substantially helical manner to form a plurality of helical windings. At least one connector member extends between longitudinally adjacent helical windings of the band.

Abstract: A biocompatible material may be configured into any number of implantable medical devices including intraluminal stents. Polymeric materials may be utilized to fabricate any of these devices, including stents. The stents may be balloon expandable or self-expanding. By preferential mechanical deformation of the polymer, the polymer chains may be oriented to achieve certain desirable performance characteristics.

Abstract: A biocompatible material may be configured into any number of implantable medical devices including intraluminal stents. Polymeric materials may be utilized to fabricate any of these devices, including stents. The stents may be balloon expandable or self-expanding. By preferential mechanical deformation of the polymer, the polymer chains may be oriented to achieve certain desirable performance characteristics.

Abstract: The present invention relates to tissue-supporting medical devices and drug delivery systems, and more particularly to tubular flexible stents that are implanted within a body lumen of a living animal or human to support the organ, maintain patency and/or deliver drugs or agents. The tubular flexible stent has a cylindrical shape defining a longitudinal axis and includes a helical section having of a plurality of longitudinally oriented strut members and a plurality of circumferentially oriented hinge members connecting circumferentially adjacent strut members to form a band. The band is wrapped about the longitudinal axis in a substantially helical manner to form a plurality of helical windings. At least one connector member extends between longitudinally adjacent helical windings of the band.

Abstract: An apparatus for compressing a coiled stent having at least one protrusion, such as an enlarged coil disposed at the end of the stent, has a mandrel insertable into a lumen of the stent for holding the stent by friction and a coil compressor coupled to the mandrel. The mandrel is rotatable on an axis relative to the coil compressor and the coil compressor has a tab extending therefrom towards the mandrel. A stent is placed on the mandrel with the enlarged coil extending toward the coil compressor. The tab presses the enlarged coil inwardly toward the lumen of the stent when the mandrel is rotated relative to the coil compressor.

Abstract: Systems and methods for fatigue testing one or more stents based on measured electrical resistance levels of each stent. Pairs of lead lines from an ohmmeter are connected to a respective stent. The respective stent is mounted onto an expander having an interior tapered portion into which a correspondingly tapered expansion pin is received. Cyclic loading strains are applied to the respective stent as an expansion pin is inserted into a corresponding one of the expanders. Stent fracture or failure occurs when cyclic loading exceeds the stents architectural and material capacity. Such fracture fatigue or failure is identified by increased electrical resistance levels. Resistance may be continuously monitored to more readily identify the onset of fatigue or failure. The expansion pins extend from a movable plate, and the expanders comprise a part of corresponding stations that extend from a fixed plate.

Abstract: Systems and methods for fatigue testing one or more stents based on measured electrical resistance levels of each stent. Pairs of lead lines from an ohmmeter are connected to a respective stent. The respective stent is mounted onto an expander having an interior tapered portion into which a correspondingly tapered expansion pin is received. Cyclic loading strains are applied to the respective stent as an expansion pin is inserted into a corresponding one of the expanders. Stent fracture or failure occurs when cyclic loading exceeds the stents architectural and material capacity. Such fracture fatigue or failure is identified by increased electrical resistance levels. Resistance may be continuously monitored to more readily identify the onset of fatigue or failure. The expansion pins extend from a movable plate, and the expanders comprise a part of corresponding stations that extend from a fixed plate.

Abstract: A biocompatible material may be configured into any number of implantable medical devices including intraluminal stents. Polymeric materials may be utilized to fabricate any of these devices, including stents. The stents may be balloon expandable or self-expanding. The polymeric materials may include additives such as drugs or other bioactive agents as well as radiopaque agents. By preferential mechanical deformation of the polymer, the polymer chains may be oriented to achieve certain desirable performance characteristics.

Abstract: A surgical anchor inserter is equipped to receive or hold two or more bone anchors or the like. A corresponding number of ejection mechanisms can be actuated in concert to simultaneously deploy the anchors.

Abstract: A bone anchor for securing sutures or cables within a hole opening in a bone includes a screw element and a washer, which is separate from and independent of the screw element. The end of the cable to be secured within the bone hole opening is knotted or otherwise secured to the washer, thereby isolating the cable from the twisting of the screw element during insertion of the anchoring device into the hole opening in the bone.

Abstract: A bone anchoring device for securing suture or cable within a bone hole opening of a bone includes a radially expandable sheath, an expander member for expanding the sheath and a washer. The cable or suture is secured within the bone hole opening such that an end tip thereof is knotted or secured to the washer to prevent separation therefrom. The cable or suture is not affected by the bearing load placed on the expander member during anchor deployment, and the bearing load acting on the cable member is transferred through the washer to the sheath, and not to the expander member.

Abstract: An orthopedic interference screw has a hard, self-threading front section and a bioabsorbable rear section. The two sections are conjoined and threaded such that the hard front section cuts threads into the bone and the softer rear section follows the threads into the bone. Preferably, the screw has an axial bore for matingly receiving a turning tool such as a hex wrench.

Abstract: A bioabsorbable rivet and pin fastener is formed as an elongated unit that may be used for anchoring, or for attachment of a fixation plate. The rivet has a head mechanically connected to two or more legs that extend generally distally from the head and may flex outwardly from a central rivet axis. The pin is integral with the rivet and oriented along the central axis by a connection such as a web or a plurality of braces, forming an integral, aligned, one-piece assembly that may, for example, be molded as a single piece. The connection breaks under force as the pin is driven into the rivet, so that the pin contacts internal surfaces of the legs and pushes the legs outward into frictional engagement with the surrounding bone. The one-piece assembly may be formed in a gated mold having a central pin with a relief passage that defines the braces between upper and lower portions of the rivet.

Abstract: A surgical anchor inserter is equipped to receive or hold two or more bone anchors or the like. A corresponding number of ejection mechanisms can be actuated in concert to simultaneously deploy the anchors.

Abstract: An intramedullary nail has a dynamization opening that accommodates and utilizes a dynamization window insert. The dynamization window insert is press-fit into the dynamization opening. The dynamization window insert is oval shaped and includes first and second protrusions that extend from respective surfaces of the dynamization window insert. The dynamization opening is sized to receive the dynamization window insert but compress the protrusions/window insert during insertion. The dynamization opening includes channels or grooves that are sized to accommodate the protrusions and allow the protrusions/window insert to return to an uncompressed state when situated therein. The dynamization opening and window insert cooperate to allow a press fit of the window insert into the dynamization opening with an elastic snap-fit and audible sound.