Knee implant

• US 20060190086A1
• Filed: 12/30/2005
• Published: 08/24/2006
• Est. Priority Date: 02/22/2005
• Status: Abandoned Application

• Current Assignee: MAKO Surgical Corporation (Stryker Corporation)
• Original Assignee: MAKO Surgical Corporation (Stryker Corporation)
• Inventors: Mears, Dana C., Clemow, Alastair J.T.
• Application Number:
  US11/321,741
• Publication Number:
  US 20060190086A1
• Time in Patent Office: Days
• US Class Current: 623/20.15
• CPC Class Codes: A61F 2/38 for elbows or knees
• CPC Class Codes: A61F 2002/30604 modular
• CPC Class Codes: A61F 2002/3895 unicompartimental

Abstract

A modular prosthetic device is provided for replacement of the knee. The device is assembled from a plurality of components, each of which can be inserted through a small incision. After inserting the components through the incision, the device can be assembled within the knee cavity. The modularity of the device enables a surgeon to replace only those regions of the knee that are diseased or damaged, thereby avoiding a complete knee replacement. If, at a later time, additional regions of the knee become diseased or damaged, those additional regions of the knee can be replaced by additional device components and those additional components can be connected to the previously implanted components. By replacing only those regions of the knee that are diseased or damaged and by implanting each of the components through the small incision, the surgery is minimally invasive and, therefore, requires reduced time for healing and rehabilitation.

Claims

1. A method of implanting a prosthetic device comprising the steps of:

selecting a first side femoral component configured to be implanted on at least one of a lateral condyle and a medial condyle of a femur;

implanting the first side femoral component on one of the lateral condyle and the medial condyle of the femur;

selecting a second side femoral component configured to be implanted on at least the other of the lateral condyle and the medial condyle of the femur, wherein the second side femoral component is selected from a plurality of femoral components configured to be used with the first side femoral component based on characteristics of the second side femoral component; and

implanting the second side femoral component on the femur.

2. The method of claim 1, wherein the characteristics of the second side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

3. The method of claim 1, wherein the step of selecting the first side femoral component includes selecting from a plurality of femoral components configured to be used with the second side femoral component based on characteristics of the first side femoral component.

4. The method of claim 3, wherein the characteristics of the first side femoral component include at least one of size, condylar geometry, material, material, augment presence, and replaceability.

5. The method of claim 1, wherein the steps of implanting include inserting the first and second side femoral components through an opening in a patient'"'"'s skin of no greater than approximately two inches.

6. The method of claim 1, further comprising the step of:

connecting the first side femoral component to the second side femoral component.

7. The method of claim 1, further comprising the steps of:

selecting a center femoral component configured to be implanted on a central region of the femur, wherein the center femoral component is selected from a plurality of femoral components configured to be used with the first and second side femoral components based on characteristics of the center femoral component; and

implanting the center femoral component on the femur.

8. The method of claim 7, wherein the characteristics of the center femoral component include at least one of depth of patella-femoral groove, anatomic coverage, and cruciate compatibility.

9. The method of claim 7, wherein the step of implanting includes inserting the center femoral component through an opening in a patient'"'"'s skin of no greater than approximately two inches.

10. The method of claim 7, further comprising the steps of:

connecting the first side femoral component to the center femoral component; and

connecting the center femoral component to the second side femoral component.

11. A method of implanting a prosthetic device comprising the steps of:

selecting a first side femoral component configured to be implanted on at least one of a lateral condyle and a medial condyle of a femur;

implanting the first side femoral component on one of the lateral condyle and the medial condyle of the femur;

selecting a center femoral component configured to be implanted on a central region of the femur, wherein the center femoral component is selected from a plurality of femoral components configured to be used with the first side femoral component based on characteristics of the center femoral component; and

implanting the center femoral component on the femur.

12. The method of claim 11, wherein the characteristics of the center femoral component include at least one of depth of patella-femoral groove, anatomic coverage, and cruciate compatibility.

13. The method of claim 11, wherein the step of selecting the first side femoral component includes selecting from a plurality of femoral components configured to be used with the center femoral component based on characteristics of the first side femoral component.

14. The method of claim 13, wherein the characteristics of the first side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

15. The method of claim 11, wherein the steps of implanting include inserting the first side and center femoral components through an opening in a patient'"'"'s skin of no greater than approximately two inches.

16. The method of claim 11, further comprising the step of:

connecting the first side femoral component to the center femoral component.

17. A method of implanting a prosthetic device comprising the steps of:

selecting a first side tibial component configured to be implanted on at least one of a lateral region and a medial region of a tibia;

implanting the first side tibial component on one of the lateral region and the medial region of the tibia;

selecting a second side tibial component configured to be implanted on at least the other of the lateral region and the medial region of the tibia, wherein the second side tibial component is selected from a plurality of tibial components configured to be used with the first side tibial component based on characteristics of the second side tibial component; and

implanting the second side tibial component on the tibia.

18. The method of claim 17, wherein the characteristics of the second side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

19. The method of claim 17, wherein the step of selecting the first side tibial component includes selecting from a plurality of tibial components configured to be used with the second side tibial component based on characteristics of the first side tibial component.

20. The method of claim 19, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

21. The method of claim 17, wherein the steps of implanting include inserting the first and second side tibial components through an opening in a patient'"'"'s skin of no greater than approximately two inches.

22. The method of claim 17, further comprising the steps of:

connecting the first side tibial component to the second side tibial component.

23. The method of claim 17, further comprising the steps of:

selecting a center tibial component configured to be implanted on a central region of the tibia, wherein the center tibial component is selected from a plurality of tibial components configured to be used with the first and second side tibial components based on characteristics of the center tibial component; and

implanting the center tibial component on the tibia.

24. The method of claim 23, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

25. The method of claim 23, wherein the step of implanting includes inserting the center tibial component through an opening in a patient'"'"'s skin of no greater than approximately two inches.

26. The method of claim 23, further comprising the steps of:

connecting the first side tibial component to the center tibial component; and

connecting the center tibial component to the second side tibial component.

27. A method of implanting a prosthetic device comprising the steps of:

selecting a first side tibial component configured to be implanted on at least one of a lateral region and a medial region of a tibia;

implanting the first side tibial component on one of the lateral region and the medial region of the tibia;

selecting a center tibial component configured to be implanted on a central region of the tibia, wherein the center tibial component is selected from a plurality of tibial components configured to be used with the first side tibial component based on characteristics of the center tibial component; and

implanting the center tibial component on the tibia.

28. The method of claim 27, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

29. The method of claim 27, wherein the step of selecting the first side tibial component includes selecting from a plurality of tibial components configured to be used with the center tibial component based on characteristics of the first side tibial component.

30. The method of claim 29, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

31. The method of claim 27, wherein the steps of implanting include inserting the first side and center tibial components through an opening in a patient'"'"'s skin of no greater than approximately two inches.

32. The method of claim 27, further comprising the step of:

connecting the first side tibial component to the center tibial component.

33. A prosthetic device comprising:

a first side femoral component configured to be implanted on at least one of a lateral condyle and a medial condyle of a femur;

a second side femoral component configured to be implanted on at least the other of the lateral condyle and the medial condyle of the femur, wherein the second side femoral component is selected from a plurality of femoral components configured to be used with the first side femoral component based on characteristics of the second side femoral component.

34. The prosthetic device of claim 33, wherein the characteristics of the second side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

35. The prosthetic device of claim 33, wherein the first side femoral component is selected from a plurality of femoral components configured to be used with the second side femoral component based on characteristics of the first side femoral component.

36. The prosthetic device of claim 35, wherein the characteristics of the first side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

37. The prosthetic device of claim 33, wherein each of the femoral components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

38. The prosthetic device of claim 33, further comprising:

a mechanism for connecting the first side femoral component to the second side femoral component.

39. The prosthetic device of claim 33, further comprising:

a center femoral component configured to be implanted on a central region of the femur, wherein the center femoral component is selected from a plurality of femoral components configured to be used with the first and second side femoral components based on characteristics of the center femoral component.

40. The prosthetic device of claim 39, wherein the characteristics of the center femoral component include at least one of depth of patella-femoral groove, anatomic coverage, and cruciate compatibility.

41. The prosthetic device of claim 39, wherein each of the femoral components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

42. The prosthetic device of claim 39, further comprising:

a mechanism for connecting the first side femoral component to the center femoral component; and

a mechanism for connecting the center femoral component to the second side femoral component.

43. A prosthetic device comprising:

a first side femoral component configured to be implanted on at least one of a lateral condyle and a medial condyle of a femur; and

a center femoral component configured to be implanted on a central region of the femur, wherein the center femoral component is selected from a plurality of femoral components configured to be used with the first side femoral component based on characteristics of the center femoral component.

44. The prosthetic device of claim 43, wherein the characteristics of the center femoral component include at least one of depth of patella-femoral groove, anatomic coverage, and cruciate compatibility.

45. The prosthetic device of claim 43, wherein the first side femoral component is selected from a plurality of femoral components configured to be used with the center femoral component based on characteristics of the first side femoral component.

46. The prosthetic device of claim 45, wherein the characteristics of the first side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

47. The prosthetic device of claim 43, wherein each of the femoral components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

48. The prosthetic device of claim 43, further comprising:

a mechanism for connecting the first side femoral component to the center femoral component.

49. A prosthetic device comprising:

a first side tibial component configured to be implanted on at least one of a lateral region and a medial region of a tibia; and

a second side tibial component configured to be implanted on at least the other of the lateral region and the medial region of the tibia.

50. The prosthetic device of claim 49, wherein the first side tibial component is selected from a plurality of tibial components configured to be used with the second side tibial component based on characteristics of the first side tibial component.

51. The prosthetic device of claim 49, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

52. The prosthetic device of claim 49, wherein the second side tibial component is selected from a plurality of tibial components configured to be used with the first side tibial component based on characteristics of the second side tibial component.

53. The prosthetic device of claim 52, wherein the characteristics of the second side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

54. The prosthetic device of claim 49, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

55. The prosthetic device of claim 49, further comprising:

a mechanism for connecting the first side tibial component to the second side tibial component.

56. The prosthetic device of claim 49, wherein each of the tibial components includes a backing tray and a contact member.

57. The prosthetic device of claim 49, further comprising:

a center tibial component configured to be implanted on a central region of the tibia.

58. The prosthetic device of claim 57, wherein the center tibial component is selected from a plurality of tibial components configured to be used with the first and second side tibial components based on characteristics of the center tibial component.

59. The prosthetic device of claim 58, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

60. The prosthetic device of claim 57, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

61. The prosthetic device of claim 57, wherein each of the tibial components includes a backing tray and a contact member.

62. The prosthetic device of claim 57, further comprising:

a mechanism for connecting the first side tibial component to the center tibial component; and

a mechanism for connecting the center tibial component to the second side tibial component.

63. A prosthetic device comprising:

a first side tibial component configured to be implanted on at least one of a lateral region and a medial region of a tibia; and

a center tibial component configured to be implanted on a central region of the tibia, wherein the center tibial component is selected from a plurality of tibial components configured to be used with the first side tibial component based on characteristics of the center tibial component.

64. The prosthetic device of claim 63, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

65. The prosthetic device of claim 63, wherein the first side tibial component is selected from a plurality of tibial components configured to be used with the center tibial component based on characteristics of the first side tibial component.

66. The prosthetic device of claim 65, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

67. The prosthetic device of claim 63, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

68. The prosthetic device of claim 63, further comprising:

a mechanism for connecting the first side tibial component to the center tibial component.

69. The prosthetic device of claim 63, wherein each of the tibial components includes a backing tray and a contact member.

70. A collection of components for forming a prosthetic device, comprising:

a plurality of first side femoral components configured to be implanted on at least one of a lateral condyle and a medial condyle of a femur and having different characteristics; and

a plurality of second side femoral component configured to be implanted on at least the other of the lateral condyle and the medial condyle of the femur and having different characteristics, wherein the second side femoral components can be used with the first side femoral components.

71. The collection of claim 70, wherein the characteristics of the first side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

72. The collection of claim 70, wherein the characteristics of the second side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

73. The collection of claim 70, wherein each of the femoral components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

74. The collection of claim 70, further comprising:

a plurality of center femoral components configured to be implanted on a central region of the femur and having different characteristics, wherein the center femoral components can be used with the first and second side femoral components.

75. The collection of claim 74, wherein the characteristics of the center femoral component include at least one of depth of patella-femoral groove, anatomic coverage, and cruciate compatibility.

76. The collection of claim 74, wherein each of the femoral components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

77. A collection of components for forming a prosthetic device comprising:

a plurality of first side femoral components configured to be implanted on at least one of a lateral condyle and a medial condyle of a femur and having different characteristics; and

a plurality of center femoral components configured to be implanted on a central region of the femur and having different characteristics, wherein the center femoral components can be used with the first side femoral components.

78. The collection of claim 77, wherein the characteristics of the first side femoral component include at least one of size, condylar geometry, material, augment presence, and replaceability.

79. The collection of claim 77, wherein the characteristics of the center femoral component include at least one of depth of patella-femoral groove, anatomic coverage, and cruciate compatibility.

80. The collection of claim 77, wherein each of the femoral components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

81. The collection of claim 77, further comprising:

a plurality of first side tibial components configured to be implanted on at least one of a lateral region and a medial region of a tibia and having different characteristics; and

a plurality of second side tibial component configured to be implanted on at least the other of the lateral region and the medial region of the tibia and having different characteristics, wherein the second side tibial components can be used with the first side tibial components.

82. The collection of claim 81, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

83. The collection of claim 81, wherein the characteristics of the second side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

84. The collection of claim 81, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

85. The collection of claim 81, further comprising:

a plurality of center tibial components configured to be implanted on a central region of the tibia and having different characteristics, wherein the center tibial components can be used with the first and second side tibial components.

86. The collection of claim 85, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

87. The collection of claim 85, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

88. A collection of components for forming a prosthetic device, comprising:

a plurality of first side tibial components configured to be implanted on at least one of a lateral region and a medial region of a tibia and having different characteristics; and

a plurality of second side tibial component configured to be implanted on at least the other of the lateral region and the medial region of the tibia and having different characteristics, wherein the second side tibial components can be used with the first side tibial components.

89. The collection of claim 88, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

90. The collection of claim 88, wherein the characteristics of the second side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

91. The collection of claim 88, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

92. The collection of claim 88, further comprising:

a plurality of center tibial components configured to be implanted on a central region of the tibia and having different characteristics, wherein the center tibial components can be used with the first and second side tibial components.

93. The collection of claim 92, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

94. The collection of claim 92, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

95. The collection of claim 88, further comprising:

a tibial tray post configured to be connected to at least one of the first and second side tibial components.

96. A collection of components for forming a prosthetic device comprising:

a plurality of first side tibial components configured to be implanted on at least one of a lateral region and a medial region of a tibia and having different characteristics; and

a plurality of center tibial components configured to be implanted on a central region of the tibia and having different characteristics, wherein the center tibial components can be used with the first side tibial components.

97. The collection of claim 96, wherein the characteristics of the first side tibial component include at least one of size, condylar geometry, material, augment presence, thickness, and number of bearing surfaces.

98. The collection of claim 96, wherein the characteristics of the center tibial component include at least one of cruciate compatibility, stem interchangeability, and cruciform interchangeability.

99. The collection of claim 96, wherein each of the tibial components is configured to be implanted in a patient by insertion through an opening in the patient'"'"'s skin of no greater than approximately two inches.

100. The collection of claim 96, further comprising:

a tibial tray post configured to be connected to at least one of the first side and center tibial components.

101. A method of implanting a prosthetic device comprising the steps of:

evaluating a knee of a patient including a previously implanted prosthetic device;

implanting in the knee an additional component of a prosthetic device adjacent the previously implanted prosthetic device, while maintaining in the knee at least a portion of the previously implanted prosthetic device; and

attaching the additional component to the maintained portion of the previously implanted prosthetic device.