Abstract: Systems, apparatuses and methods for preserving motion in an intervertebral disc. Modular disc implant segments can be constructed from a relatively rigid material with compressive spring lobes to act similar to an elastomer. The lobes may be configured to have a C-shaped outer wall and one or more spring arms, such as a leaf springs, to facilitate the modular disc implant segment's ability to compress, thereby enabling an entire intervertebral disc constructed from multiple modular disc implant segments to compress with the implant recipient's movement. The implant segments are sized to be inserted serially into a space defined by the annular fibrosus after removal of the nucleus pulposus with connections being made between adjacent segments in the space during the insertion process.

Abstract: Methods and devices of tissue attachment with one or more tissue layers being attached using an adhesive to bone or other tissue layers including moving skin and surrounding tissues of the face or any other body part in relationship to the bone or cartilage structures below thus effecting a “skin tightening” or lifting procedure. Methods and devices for minimally invasively locating a precise tissue layer, repositioning the tissue layer in relation to the surrounding tissue layers, creating a specific potential space, delivering an adhesive material within the tissue and depositing an amount of adhesive/sealant material to allow for tissue adhesion.

Abstract: Methods and devices of tissue attachment with one or more tissue layers being attached using an adhesive to bone or other tissue layers including moving skin and surrounding tissues of the face or any other body part in relationship to the bone or cartilage structures below thus effecting a “skin tightening” or lifting procedure. Methods and devices for minimally invasively locating a precise tissue layer, repositioning the tissue layer in relation to the surrounding tissue layers, creating a specific potential space, delivering an adhesive material within the tissue and depositing an amount of adhesive/sealant material to allow for tissue adhesion.

Abstract: A modular interbody fusion device for fusing adjacent spinal vertebrae that is adapted to be implanted in a prepared interbody space including a first modular segment having a width including a first rail extending at least partially along one side of the width and beyond a periphery of a body portion of the first modular segment, a second modular segment having a width and slidably connected to the first rail on one side of the width and having a second rail extending at least partially along another side of the width and beyond a periphery of a body portion of the second modular segment, a third modular segment having a width and slidably connected to the second rail on one side of the width and wherein the device has an expanded position and an implanted position in which the modular segments are combined to mimic the shape of the vertebra.

Abstract: The invention is a modular interbody fusion device for fusing adjacent spinal vertebrae that is adapted to be implanted in a prepared interbody space including a first modular segment having a width including a first rail extending at least partially along one side of the width and beyond a periphery of a body portion of the first modular segment, a second modular segment having a width and slidably connected to the first rail on one side of the width and having a second rail extending at least partially along another side of the width and beyond a periphery of a body portion of the second modular segment, a third modular segment having a width and slidably connected to the second rail on one side of the width and wherein the device has an expanded position in which the second and third modular segments are extended along the first and second rails and positioned in a generally end to end configuration spaced apart by the rails prior to implantation and an implanted position in which the modular segments are

Abstract: The present invention is an intervertebral disc replacement for replacing a disc between a first vertebra and a second vertebra including an upper containment structure adapted to contact a lower surface of a first vertebra, a lower containment structure adapted to contact an upper surface of a second vertebra, where the upper and lower containment structures are adapted to centrally contain a deformable support body positioned between the upper and lower containment structures.

Abstract: The invention includes an interpositional arthrosplasty implant adapted to be retained in position in apposition to ajoint surface, at least in part, by surrounding healthy tissue. In some embodiments the implant comprises a knee implant. The implant can include one or more structural features adapted to be fixedly positioned within and/or in apposition to the natural meniscus.

Abstract: A method and apparatus for repairing a damaged intervertebral disc nucleus in a minimally invasive manner utilizes a modular disc prosthesis. The modular disc prosthesis preferably comprises at least three modular segments. In one embodiment, each modular segment includes an inner core and an outer shell. The modular segments are selectively interlockable in situ with each other. The modular segments form an implanted unitary device that closely mimics the geometry of the disc nucleus cavity.

Abstract: An interpositional arthroplasty system for use in repairing ginglymus joints such as the joints of the ankle, including a tibiotalar implant (124) that provides a first major surface (130) adapted to be positioned against a tibia (120) and a second major surface (132) adapted to be positioned against a talus (108) and a polymeric ankle implant that provides a first major surface adapted to be positioned against a talus and a second major surface adapted to be positioned against a calcaneus. Such an implant can be useful for correcting various deformities of an ankle, as well as increasing articulation of a joint. Also described are biomaterials, including polymeric biomaterials having use in preparing such implants, as well as surgical kits that include implants and other tools adapted for their use.

Abstract: The invention can provide an implant for an upper extremity joint arthroplasty having a first polymeric portion adapted to be retained within a bone of the upper extremity and a second polymeric portion having an articulating surface adapted to articulate against an opposing bone. The invention can also provide methods of making and using such an implant.

Abstract: A catheter holder designed to deliver a curable biomaterial to an intervertebral disc space. By securing the catheter to the catheter holder, the depth of insertion of the catheter into the disc space can be accurately controlled. The catheter holder optionally helps with insertion of a optional mold through the annulotomy and into the disc space created by the nuclectomy. The catheter holder helps keep the mold from being drawn too far into the disc space or pushed too far out of the disc space during polymer injection.

Abstract: A system for the creation or modification of an orthopedic joint within a mammalian body is disclosed. The system includes an implant (122, 132, 232, 332, 432) that provides a major surface adapted to be positioned against a metatarsal bone and an end (136, 236, 336, 436) adapted to be retained within a phalange.

Abstract: A method and system for the creation or modification of the wear surface of orthopedic joints, involving the preparation and use of one or more partially or fully preformed components adapted for insertion and placement into the body and at the joint site. The system includes a method and related components and/or devices in the form of a kit that can be used to provide or perform some or all of the steps of: a) preparing a joint to receive an implant, b) determining an appropriate implant size for a particular joint, c) determining an appropriate implant thickness, d) inserting the implant into the joint, and/or e) securing the implant within the joint to a desired extent. One or more of the various components and devices, including optionally one or more implants themselves, can be provided or packaged separately or in varying desired combinations and subcombinations to provide a kit of this invention.

Abstract: A method and apparatus is described that includes a catheter and a penetrating member at a distal end of the catheter for penetrating a tissue. The penetrating member can have a lumen in communication with the catheter, the lumen having an opening at a surface of the penetrating member to deliver a substance through the lumen. The device includes means for determining a location of the opening relative to the tissue.

Abstract: An apparatus and method for imparting rejuvenating energy to the skin uses a handheld ergonomic apparatus with selectable treatment components to achieve tuned energy application to a portion of the dermal layer of a user.

Abstract: A method and system for preparing a bone surface, as by smoothing the surface, in preparation for contacting and/or receiving a prosthetic implant. The smoothing system and method are particularly well suited for use with articulating joints, in which a polymeric biomaterial such as polyurethane is implanted and retained upon one (supporting) bone surface, in order to provide a corresponding surface for opposing, articulating bone. Smoothing condylar bone, for instance, can significantly decrease the friction between a the condylar surface, and particularly one that is itself diseased or damaged, and to remove osteophytes and entheseophytes.

Abstract: A polymer intravascular stent that is resorable over a period of time containing a drug, which is delivered to the vascular wall during the absorption of the polymer material. A gradient of drug concentration may be established in the polymer.

Abstract: A method, and related composition and apparatus for repairing a tissue site. The method involves the use of a curable polyurethane biomaterial composition having a plurality of parts adapted to be mixed at the time of use in order to provide a flowable composition and to initiate cure. The flowable composition can be delivered using minimally invasive means to a tissue site and there fully cured provide a permanent and biocompatible prosthesis for repair of the tissue site. Further provided are a mold apparatus, e.g., in the form of a balloon or tubular cavity, for receiving a biomaterial composition, and a method for delivering and filling the mold apparatus with a curable composition in situ to provide a prosthesis for tissue repair.

Abstract: An apparatus includes a catheter for insertion into a stomach to introduce air into the stomach through the catheter and a pressure measurement device associated with the catheter to sense a pressure in the stomach. The pressure measurement device is used to determine a gastric yield pressure of the stomach when enough air has been introduced to the stomach to overcome the esophageal-gastric junction.