Howmedica Osteonics Corporation

Christopher DeMaria

Philip F Williams, Iii

Chau Ngo

Paul Higham

Thomas Francis McCarthy

Anthony J La Rosa

Edward J Laganis

Jason R Cahayla

The present invention relates to a femoral component for use in connection with knee anthroplasty. The implant includes a support having a contoured inner bone engaging surface, and a shell affixed to the support. The shell has an outer surface spaced so as to provide an articulation surface for engaging the tibia that substantially replicates the shape of a femoral condyle, and an inner surface for receiving an outer surface of the support. The support bone engaging surface is structured to mate with a prepared surface of the distal femur and the support spaces the shell outer surface at a predetermined distance from the prepared surface.

Composite joint implant

A spinal implant for replacing the natural nucleus of the disc made from a polymer such as hydrogel having a radiopaque material located within the polymer. The material may be in the form of a powder dispersed throughout the polymer or may be in he form of a powder dispersed in layers or in other specific locations within the polymer. The radiopaque material is metal such as gold, tungsten, titanium, tantalum or platinum. The metal may also be in the form of a foil or wire located within the hydrogel such as polyurethane, thereby making the implant visible on x-rays. Other polymers besides hydrogel may be used with the radiopaque material being dispersed therein.

Radiovisible hydrogel intervertebral disc nucleus

An orthopedic reamer for use in creating and sizing canals in a bone is disclosed. The orthopedic reamer includes a non-polymeric cutting portion having at least one cutting surface thereon and a polymeric body portion covering at least a portion of the cutting portion. The at least one cutting surface is not covered by the polymeric body portion.

Orthopedic reamer

Apparatus and method are described for interoperatively determining, during a trailing procedure conducted in connection with total hip arthroplasty, a combination of neck length and femoral head offset required in a femoral component for establishing appropriate hip mechanics in a prosthetic hip joint to be implanted at an implant site. A trial femoral head is coupled for selective movement relative to a femoral stem component to move the trial femoral head longitudinally and laterally relative to a predetermined direction among selected combinations of trial distance and trial offset to evaluate hip mechanics and determine interoperatively an appropriate combination of trial distance and trial offset corresponding to the combination of neck length and femoral head offset required in the prosthetic hip joint.

Hip arthroplasty trialing apparatus with adjustable proximal trial and method

A wear resistant hydrogel for use as a prosthetic implant, such as for cartilage, is made by forming a solution of polyvinyl alcohol in a solvent of DMSO/water. The solution is placed in a mold and is gelated by cycling the mold in a freeze-thaw cycle at a temperature at or below 4&#xb0; C. for a period of 2 to 24 hours. The hydrogel so formed is washed in a saline solution, including potassium carbonate. The hydrogel is then dehydrated to 20 to 70% water content and thereafter irradiated with Gamma radiation. The surface of the hydrogel is then cross-linked using a boric acid solution preferably between 2.5 and 5% for about 1 minute. The hydrogel is then rinsed and sterilized.

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Glen Rock, NJ, United States of America

Christopher DeMaria