Abstract: Magnetic-based electronic valve readers for determining a location and orientation of magnets coupled to implantable medical devices to determine a setting of the device (e.g., setting of a fluid flow control valve of the medical device). The electronic valve readers include an orientation sensing mechanism that is provided and configured to enable the electronic valve reader to: 1) allow for internal offset calculation of an orientation change of the electronic valve reader during a reading process; and/or 2) during the reading process, provide an indication or warning to the clinician that the orientation of the electronic valve reader has changed to an extent at or exceeding a predetermined angular acceptance threshold or window. Systems including the disclosed electronic valve readers and methods of reading a setting of the device are also disclosed.

Abstract: Magnetic-based electronic valve readers for determining a location and orientation of magnets coupled to implantable medical devices to determine a setting of the device (e.g., setting of a fluid flow control valve of the medical device). The electronic valve readers include an orientation sensing mechanism that is provided and configured to enable the electronic valve reader to: 1) allow for internal offset calculation of an orientation change of the electronic valve reader during a reading process; and/or 2) during the reading process, provide an indication or warning to the clinician that the orientation of the electronic valve reader has changed to an extent at or exceeding a predetermined angular acceptance threshold or window. Systems including the disclosed electronic valve readers and methods of reading a setting of the device are also disclosed.

Abstract: Magnetic-based electronic valve readers for determining a location and orientation of magnets coupled to implantable medical devices to determine a setting of the device (e.g., setting of a fluid flow control valve of the medical device). The electronic valve readers include an orientation sensing mechanism that is provided and configured to enable the electronic valve reader to: 1) allow for internal offset calculation of an orientation change of the electronic valve reader during a reading process; and/or 2) during the reading process, provide an indication or warning to the clinician that the orientation of the electronic valve reader has changed to an extent at or exceeding a predetermined angular acceptance threshold or window. Systems including the disclosed electronic valve readers and methods of reading a setting of the device are also disclosed.

Abstract: Magnetic-based electronic valve readers for determining a location and orientation of magnets coupled to implantable medical devices to determine a setting of the device (e.g., setting of a fluid flow control valve of the medical device). The electronic valve readers include an orientation sensing mechanism that is provided and configured to enable the electronic valve reader to: 1) allow for internal offset calculation of an orientation change of the electronic valve reader during a reading process; and/or 2) during the reading process, provide an indication or warning to the clinician that the orientation of the electronic valve reader has changed to an extent at or exceeding a predetermined angular acceptance threshold or window. Systems including the disclosed electronic valve readers and methods of reading a setting of the device are also disclosed.

Abstract: Magnetic-based electronic valve readers for determining a location and orientation of magnets coupled to implantable medical devices to determine a setting of the device (e.g., setting of a fluid flow control valve of the medical device). The electronic valve readers include an orientation sensing mechanism that is provided and configured to enable the electronic valve reader to: 1) allow for internal offset calculation of an orientation change of the electronic valve reader during a reading process; and/or 2) during the reading process, provide an indication or warning to the clinician that the orientation of the electronic valve reader has changed to an extent at or exceeding a predetermined angular acceptance threshold or window. Systems including the disclosed electronic valve readers and methods of reading a setting of the device are also disclosed.

Abstract: A drug-eluting device comprising a drug-eluting matrix containing at least one elutable drug, a method of manufacturing a preformed drug-eluting device, and an implant kit comprising the same.

Abstract: Drug loading of polymeric materials can be adjusted by selection of materials and/or adjusting processing steps in formation of an implantable drug-loaded device.

Abstract: An osteotomy system, typically for tibial alignment correction, includes a wedge implant and an osteotomy guide. The wedge implant is generally U-shaped and its upper and lower surfaces may be inclined with respect to one another in two orthogonal planes to correct respective misalignments. The osteotomy guide controls cutting of the osteotomy opening and the drilling of a hole defining the apex of the osteotomy, forming a bony hinge about which the osteotomy may be opened.

Abstract: Drug loading of polymeric materials can be adjusted by selection of materials and/or adjusting processing steps in formation of an implantable drug-loaded device.

Abstract: A knotless suture anchor and method for its insertion into tissue are provided. The suture anchor includes an inner member including a proximal shaft and a distal securing member shaped to secure the inner member to the tissue, the proximal shaft including a first locking part and at least one hole extending therethrough for receiving the suture thread; and a collar member including an axial bore shaped to receive the proximal shaft of the inner member, a second locking part, and at least one hole extending therethrough and assigned to the hole of the proximal shaft of the inner member, the collar member being axially slidable into unlocked and locked positions relative to the proximal shaft of the inner member, the collar member being relatively axially slidable into the locked position only to secure the suture thread.

Abstract: A drug-eluting device comprising a drug-eluting matrix containing at least one elutable drug, a method of manufacturing a preformed drug-eluting device, and an implant kit comprising the same.

Abstract: A drug-eluting implant cover fabricated from a drug-eluting biocompatible matrix containing at least one elutable drug, a drug-eluting implant cover kit containing at least one drug-eluting implant cover, and a method of manufacturing the same.

Abstract: A tool for dilating tunnels in bone, in order to compact the cancellous bone around the tunnel and providing better holding for interference screws and the like, comprises a plurality of elongated segments mounted for radial motion with respect to an axis of elongation. When actuated, the segments move radially outwardly, parallel to the axis of elongation, compacting the bone.

Abstract: A tool for dilating tunnels in bone, in order to compact the cancellous bone around the tunnel and providing better holding for interference screws and the like, comprises a plurality of elongated segments mounted for radial motion with respect to an axis of elongation. When actuated, the segments move radially outwardly, parallel to the axis of elongation, compacting the bone.

Abstract: An osteotomy system includes a wedge implant and an osteotomy guide.

Abstract: A knotless suture anchor and method for its insertion into tissue are provided. The suture anchor includes an inner member including a proximal shaft and a distal securing member shaped to secure the inner member to the tissue, the proximal shaft including a first locking part and at least one hole extending therethrough for receiving the suture thread; and a collar member including an axial bore shaped to receive the proximal shaft of the inner member, a second locking part, and at least one hole extending therethrough and assigned to the hole of the proximal shaft of the inner member, the collar member being axially slidable into unlocked and locked positions relative to the proximal shaft of the inner member, the collar member being relatively axially slidable into the locked position only to secure the suture thread.

Abstract: A two piece graft fixation arrangement includes a graft block engageable with a graft and a transverse member engageable with the graft block to fix the graft block in a bone tunnel. Instruments and methods are presented for installing a graft in a bone tunnel and anchoring the graft with a transverse member placed through a transverse bore intersecting the bone tunnel.

Abstract: In the present invention, a gel-spun UHMWPE is subjected to secondary processing to reduce the concentration of the spin solvent(s) to acceptable levels before or after the fiber is woven with other fibers to form a suture. In the case of the spin solvent Decalin, it is well known that concentrations, in the fiber, of greater than 100 parts per million (ppm) render UHMWPE materials non-compatible with human tissues. Thus, UHMWPE materials that are to remain within the human body must have a Decalin concentration below 100 ppm to render them biocompatible. If desired, the suture may be braided about a core. The number of filaments in a single suture can vary between 4 and 24. Additionally, where a core structure is employed, up to 6 separate core filaments may be employed. Other materials such as PTFE, FEP, PFA, PVFD, PP, polyester, nylon, or aramid may be employed for the core and/or cover so long as spin solvent level has been reduced to below 100 ppm before or after twisting or braiding.

Abstract: A high strength suture is made from a LCP/polyester composite of braided filaments having a high coefficient of friction. Knots tied in a suture made from such braided filaments have a tendency to stay in place better than the prior art UHMWPE/polyester composite knots. The inventive suture may include a multifilament cover of fibers of LCP and/or LCP composite fibers. Where a core is employed, the core may be made up of twisted fibers of LCP and liquid crystal composite fibers. If desired, the composite fibers can be a combination of LCP and other polymers such as polyester, nylon, fluoropolymers such as FEP or PTFE or olefins such as polypropylene, polyethylene or UHMWPE. A low friction coating, such as silicone, may be applied over the outside surfaces of the suture.