Abstract: A method for mounting a tibial condylar implant includes forming a tunnel having a proximal end on a lateral, medial, or anterior side of a proximal end of the tibia and a distal end on an at least partially resected lateral or medial facet at the proximal end of the tibia. A condylar implant is positioned over the distal end of the tunnel. A fastener is advanced into the tunnel from the proximal end of the tunnel. The fastener which is at least partially disposed within the tunnel is secured to the condylar implant.

Abstract: A frame is attachable to first and second bone portions of a patient to facilitate measurement and resection of one or more bony landmarks. The frame has two anchoring features, each of which has a semispherical surface that permits rotational adjustment of the frame against the bone portions until the frame is secured. A bridging structure couples the anchoring features together such that the anchoring features are lockably movable with respect to each other. The bridging structure may have three linear sliders that provide the relative motion. A locking mechanism exerts pressure on all three sliders to lock them in place. An external anchoring feature enables attachment of the frame to a stationary reference to stabilize the frame. The frame also has registration features that permit attachment of measurement or resection tools to the frame. The frame is particularly useful for measuring and resecting spinal facets for facet replacement.

Abstract: A catheter connector system for a subcutaneously placed catheter. The catheter connector system permits proximal trimming of the placed catheter, which is a procedure that provides numerous advantages over traditional methods of trimming catheter distal ends prior to implantation. The catheter connector system can be configured for a single lumen catheter or a multiple lumen catheter. The catheter connector system facilitates precise positioning of both distal and proximal ends of a catheter, providing enhanced function ability and patient comfort.

Abstract: A guide assembly for forming a tunnel through a proximal end of a tibia includes a brace having a first end and an opposing second end. A template is mounted on the first end of the brace. The template is adapted to rest on a lateral or medial facet at a proximal end of the tibia. A tubular guide sleeve has a proximal end and an opposing distal end. The tubular guide sleeve is adjustably mounted on the second end of the brace such that when the template is disposed on the lateral or medial facet of the tibia, the distal end of the tubular guide sleeve can be selectively biased against a leteral, media, or anterior side of a proximal end of the tibia.

Abstract: A method for mounting a tibial condylar implant includes forming a tunnel having a proximal end on a lateral, medial, or anterior side of a proximal end of the tibia and a distal end on an at least partially resected lateral or medial facet at the proximal end of the tibia. A condylar implant is positioned over the distal end of the tunnel. A fastener is advanced into the tunnel from the proximal end of the tunnel. The fastener which is at least partially disposed within the tunnel is secured to the condylar implant.

Abstract: A method for resecting at least a portion of a lateral or medial facet at the proximal end of a tibia includes forming a tunnel having a proximal end on a lateral, medial, or anterior side of a proximal end of a tibia and a distal end on a lateral or medial facet at the proximal end of the tibia. A first end of a retention rod is advanced from the proximal end of the tunnel to the distal end of the tunnel. The first end of the retention rod is coupled to a rasp. At least the rasp or the retention rod is moved so as to cause the rasp to resect at least a portion of the lateral or medial facet of the tibia.

Abstract: Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra.

Abstract: Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra.

Abstract: Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra.

Abstract: A dilating system for dilating bodily tissue includes a elongate tubular first dilator and a elongate tubular second dilator. The second dilator has an outer diameter greater than the outer diameter of the first dilator, the first dilator being configured to be received within the second dilator. In one embodiment, a first mating member is formed on the exterior surface of the first dilator while a second mating member is formed on the interior surface of the second dilator. The first mating member engages with the second mating member when the second dilator is passed over the first dilator so as to cause the second dilator to travel along a fixed path relative to the first dilator.

Abstract: A bifurcation insert for a coaxial catheter and a catheter assembly incorporating the bifurcation insert. The bifurcation insert contains an opening at a distal end and two openings in a proximal end, the distal end being configured for positioning within a proximal end of an outer lumen of the coaxial catheter. At the proximal end of the bifurcation insert, an arterial side is configured to receive a first extension tube, while a venous side is configured to receive a second extension tube. The catheter assembly incorporating the bifurcation insert includes a hub that is molded around the insert and properly positioned extension tubes and coaxial catheter such that each component is set into place with respect to one another.

Abstract: A safety needle device and positive flush mechanism for use with a vascular access port. In one embodiment, the combination needle assembly includes a needle, a body and a base, the body being collapsible to expunge fluid therefrom as the needle is withdrawn from a vascular access port. In another embodiment, the combination needle assembly includes a needle, a housing and a reservoir, the housing squeezing the reservoir to expunge fluid therefrom as the needle is withdrawn from the port. In another embodiment, the needle assembly includes a compression plate and balloon extension, the compression plate forcing fluid out of the balloon extension as the needle is withdrawn from the port. In all embodiments, the needle assembly is configured to provide a positive flush to overcome negative pressures in the vascular access port, while also providing a locking mechanism to prevent accidental needle sticks.

Abstract: A method for mounting an implant at an orthopedic joint includes forming a tunnel through a bone, the tunnel having an open second end on a natural or resected articulating surface of the bone and an open first end at a location on the bone spaced apart from the natural or resected articulating surface. A fastener is advanced into the tunnel from the first end of the tunnel. The fastener, which is at least partially disposed within the tunnel, is then secured to the implant which is disposed over the second end of the tunnel.