Howmedica Corp.

Pfizer Hospital Products Group, Inc.

Stryker Technologies Corporation

Benoist Girard Sas

Casper F Stark

Deh-Chuan Sun

Nestor A Arroyo

Jessica Dee Posey-Dowty

Paul A Higham

Ruey Y Lin

John H Dumbleton

Aiguo Wang

Eric Jones

Raymond W Augustin

Thomas E Crippen

Ruey Lin

Missoum Moumene

A medical implant made of polymeric material having an increased oxidation resistance is formed by a method including the steps of placing a resin powder in a sealed container. A substantial portion of the oxygen is removed from the sealed contained by either a vacuum, an oxygen absorbent or by flushing with inert gas. The container is then repressurized with a gas such as nitrogen, argon, helium or neon so that long term storage may be possible. On use, the resin in transferred to a forming device which both melts and forms the resin in an oxygen reduced atmosphere to produce a polymeric raw material such as a rod or bar stock. The medical implant is then formed from this raw material annealed and sealed in an airtight package in an oxygen reduced atmosphere. The implant is then radiation sterilized and thereafter annealed in the package for a predetermined time and temperature sufficient to form cross-links between any free radicals in neighboring polymeric chains.

Non-oxidizing polymeric medical implant

According to the present invention a prosthetic bearing component is formed from a composite synthetic plastics material comprising an injection molded thermoplastic polymeric matrix reinforced by a pitch based carbon fiber and having a bearing surface which has been machined with a surface roughness with a value less than R 2 &mgr;m. Such components have shown superior wear qualities. Preferably the bearing surface shape is machined with tolerances of 0.1 to 0.15 mm. The composite material must be capable of withstanding a radiation value of at least 2.8 Mega Rads (MRad). In components in which the bearing surface is substantially or part spherical a sphericity of 0.3 &mgr;m within a solid angle of 45&deg; is required.

Prosthesis bearing component

A medical implant made of polymeric material having an increased oxidation resistance is formed by a method including the steps of placing a resin powder in a sealed container. A substantial portion of the oxygen is removed from the sealed container by either a vacuum, an oxygen absorbent or by flushing with inert gas. The container is then repressurized with a gas such as nitrogen, argon, helium or neon so that long term storage may be possible. On use, the resin is transferred to a forming device which both melts and forms the resin in an oxygen reduced atmosphere to produce a polymeric raw material such as a rod or bar stock. The medical implant is then formed from this raw material annealed and sealed in an airtight package in an oxygen reduced atmosphere. The implant is then radiation sterilized and thereafter annealed in the package for a predetermined time and temperature sufficient to form cross-links between any free radicals in neighboring polymeric chains.

A medical implant made of polymeric material having an increased oxidation resistance is formed by a method including the step of placing a resin powder in a sealed container. A substantial portion of the oxygen is removed from the sealed container by either a vacuum, an oxygen absorbent or by flushing with inert gas. The container is then repressurized with a gas such as nitrogen, argon, helium or neon so that long term storage may be possible. On use, the resin is transferred to a forming device which both melts and forms the resin in an oxygen reduced atmosphere to produce a polymeric raw material such as a rod or bar stock. The medical implant is then formed from this raw material annealed and sealed in an airtight package in an oxygen reduced atmosphere. The implant is then radiation sterilized and thereafter annealed in the package for a predetermined time and temperature sufficient to form cross-links between any free radicals in neighboring polymeric chains.

A medical implant made of polymeric material having an increased oxidation resistance is formed by a method including the steps of placing a resin powder in a sealed container. A substantial portion of the oxygen is removed from the sealed container by either a vacuum, an oxygen absorbent or by flushing with inert gas. The container is then repressurized with a gas such as nitrogen, argon, helium or neon so that long term storage may be possible. On use, the resin is transferred to a forming device which both melts and forms the resin in an oxygen reduced atmosphere to produce a polymeric raw material such as a rod or bar stock. The medical implant is then formed from this raw material annealed and sealed in an air-tight package in an oxygen reduced atmosphere. The implant is then radiation sterilized and thereafter annealed in the package for a predetermined time and temperature sufficient to form cross-links between any free radicals in neighboring polymeric chains.

Non oxidizing polymeric medical implant

A beam adapted for implantation within a bone is able to support bending and torsional loading forces applied thereto. The beam has a stiffness defined by a modulus elasticity, which stiffness varies along the length of the beam to match the corresponding stiffness of the cortical bone adjacent the beam after implantation within the bone. The beam is made from an elongated core formed of chopped carbon fibers embedded in a thermoplastic polymer matrix. Encasing the core is a sheath formed of carbon reinforced filament fibers embedded in the thermoplastic polymer which is wound in spiral formation around the core and molded thereto. The winding angle and the sheath thickness along the beam may be varied to vary the modulus of elasticity to match that of the cortical bone adjacent thereto.

Composite orthopedic implant

A bone cement is disclosed wherein the liquid component contains a therapeutic or diagnostic substance in combination with an emulsifying agent for said substance.

Bone cement for sustained release of substances

A beam adapted for implantation within a bone is able to support bending and torsional loading forces applied thereto. The beam has a stiffness defined by a modulus elasticity, which stiffness varies along the length of the beam to match the corresponding stiffness of the cortical bone adjacent the beam after implantation within the bone. The beam is made from an elongated core formed of continuous filament carbon fibers embedded in a thermoplastic polymer matrix with the carbon filaments extending in a direction substantially parallel to the longitudinal axis of the beam. Encasing the core is a filler molded to the core, which filler is made up of the same thermoplastic polymer as the core but contains no reinforcing carbon fibers. The filler provides the prosthesis with a shape generally conforming to the desired shape of the final prosthetic implant. A sheath formed of carbon reinforced filament fibers embedded in the thermoplastic polymer is wound in spiral formation around the filler and molded thereto. The winding angle and the sheath thickness along the beam may be varied to vary the modulus of elasticity to match that of the cortical bone adjacent thereto.

A method and apparatus for use in reducing the volatilization of the monomer component of bone cement is used after a prosthesis is implanted and throughout the polymerization of bone cement. The apparatus includes a generally annular inflatable sealing member having a centrally located opening therein for fitting over the exposed end of the prosthesis. The sealing member has an outer diameter covering the exposed surface of the bone cement. The sealing member has a deformable surface disposed in a substantially co-planar relationship with the exposed surface of the bone cement. The sealing member is resiliently expandable by inflation and extends beyond the edges of the bone defining the cavity, to seal the bone cavity upon the deformation of the deformable surface thereon. A pump is provided for inflating the sealing member and causing the deformable surface to apply pressure to the exposed surface of the bone cement. A valving system and a pressure gage are used for controlling the pressure applied to the exposed surface of the bone cement within a range of from 8-14 psi.

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Pompton Lakes, NJ, United States of America

Casper F Stark