Claims
- 1. A joint prosthesis for articulation, comprising:
a first component having an articulation surface formed from a biocompatible ceramic having a flexural strength greater than about 700 Mega-Pascal (MPa) and a toughness greater than about 7 Mega-Pascal root meter (MPam0.5); and a second component having an articulation surface formed from a material selected from the group consisting of a biocompatible metal and a biocompatible ceramic having a flexural strength greater than about 700 Mega-Pascal (MPa) and a toughness greater than about 7 Mega-Pascal root meter (MPam0.5).
- 2. The joint prosthesis of claim 1 wherein said biocompatible ceramic comprises doped silicon nitride.
- 3. The joint prosthesis of claim 2 wherein dopants for said doped silicon nitride are selected from the group consisting of yttrium oxide, magnesium oxide, strontium oxide, alumina, and combinations thereof.
- 4. The joint prosthesis of claim 1 wherein said biocompatible ceramic comprises Si3N4 doped with 6 weight % Y2O3+4 weight % Al2O3.
- 5. The joint prosthesis of claim 1 wherein said biocompatible ceramic is selected from the group consisting of doped silicon nitride, doped zirconia, and zirconia toughened alumina.
- 6. The joint prosthesis of claim 1 wherein said biocompatible metal comprises a cobalt chromium alloy.
- 7. The joint prosthesis of claim 1 comprising a hip prosthesis.
- 8. The joint prosthesis of claim 1 wherein said first component comprises a hip joint acetabular cup prosthesis and said second component comprises a hip joint femoral head prosthesis.
- 9. The joint prosthesis of claim 1 wherein the articulation surface of said biocompatible ceramic has a surface roughness of less than about 0.05 μm.
- 10. The joint prosthesis of claim 1 wherein the diametral clearance between articulation surfaces of said first and second components is between about 75 and about 250 μm.
- 11. The joint prosthesis of claim 10 wherein said clearance is between about 100 and about 200 μm.
- 12. The joint prosthesis of claim 1 comprising a knee prosthesis.
- 13. The joint prosthesis of claim 1 comprising a shoulder prosthesis.
- 14. The joint prosthesis of claim 1 wherein said first component is subjected substantially to compressive stresses when implanted into a patient, and wherein the articulation surface of said second component comprises a biocompatible metal and is subjected substantially to tensile stresses when implanted into a patient.
- 15. The joint prosthesis of claim 1 wherein said biocompatible metal comprises a cobalt chromium alloy having from about 0.06 to about 0.35% carbon by weight.
- 16. The joint prosthesis of claim 1 wherein said biocompatible metal an alloy having from about 58 to about 69 weight % cobalt, from about 26 to about 30 weight % chromium, from about 5 to about 7 weight % molybdenum and less than about 5 total weight % of other elements.
- 17. The joint prosthesis of claim 16 wherein said alloy further comprises up to about 1 weight % nickel, up to about 0.75 weight % iron, up to about 1 weight % silicon, up to about 1 weight % manganese and up to about 0.25 weight % nitrogen.
- 18. The joint prosthesis of claim 1 wherein said biocompatible metal comprises a wrought alloy.
- 19. The joint prosthesis of claim 18 wherein said wrought alloy conforms to ASTM specification F1537.
- 20. A hip joint prosthesis, comprising:
an acetabular cup having an articulation surface formed from a biocompatible ceramic having a flexural strength greater than about 700 Mega-Pascal (MPa) and a toughness greater than about 7 Mega-Pascal root meter (MPam0.5); and a femoral head having an articulation surface formed from a material selected from the group consisting of a biocompatible metal and a biocompatible ceramic having a flexural strength greater than about 700 Mega-Pascal (MPa) and a toughness greater than about 7 Mega-Pascal root meter (MPam0.5).
- 21. The hip joint prosthesis of claim 20 wherein said biocompatible metal comprises a cobalt chromium alloy having a carbon content in the range of from about 0.06 to about 0.35% by weight.
- 22. The hip joint prosthesis of claim 20 wherein said biocompatible ceramic comprises doped silicon nitride.
- 23. The joint prosthesis of claim 22 wherein dopants for said doped silicon nitride are selected from the group consisting of yttrium oxide, magnesium oxide, strontium oxide, alumina, and combinations thereof.
- 24. The joint prosthesis of claim 1 wherein said biocompatible ceramic comprises Si3N4 doped with 6 weight % Y2O3+4 weight % Al2O3.
- 25. The hip joint prosthesis of claim 20 wherein said biocompatible ceramic is selected from the group consisting of doped silicon nitride, doped zirconia, and zirconia toughened alumina.
- 26. The hip joint prosthesis of claim 20 wherein the articulation surface of said femoral head is formed from a cobalt chromium alloy having a carbon content ranging from about 0.06 to about 0.35 weight %.
- 27. The hip joint prosthesis of claim 20 wherein the articulation surface of said biocompatible ceramic has a surface roughness of less than about 0.05 μm.
- 28. The hip joint prosthesis of claim 20 wherein the diametral clearance between the articulation surfaces of said acetabular cup and said femoral head is between about 75 and about 250 μm.
- 29. The hip joint prosthesis of claim 28 wherein said clearance is between about 100 and about 200 μm.
- 30. The hip joint prosthesis according to claim 20 wherein the articulation surface of said femoral head has a size ranging from about 22 mm to about 44 mm.
BACKGROUND OF THE INVENTION
[0001] This application claims the benefit of U.S. Provisional Appln. No. 60/298,669, filed Jun. 14, 2001.
Provisional Applications (1)
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Number |
Date |
Country |
|
60298669 |
Jun 2001 |
US |