Orthopaedic knee prosthesis having controlled condylar curvature

Abstract
An orthopaedic knee prosthesis includes a tibial bearing and a femoral component configured to articulate with the tibial bearing. The femoral component includes a posterior cam configured to contact a spine of the tibial bearing and a condyle surface curved in the sagittal plane. The radius of curvature of the condyle surface decreases gradually between early-flexion and mid-flexion. Additionally, in some embodiments, the radius of curvature of the condyle surface may be increased during mid-flexion.
Description
CROSS-REFERENCE TO RELATED U.S. PATENT APPLICATION

Cross-reference is made to U.S. Utility patent application Ser. No. 12/165,579, now U.S. Pat. No. 8,828,086, entitled “Orthopaedic Femoral Component Having Controlled Condylar Curvature” by John L. Williams et al., which was filed on Jun. 30, 2008; to U.S. Utility patent application Ser. No. 12/165,574, now U.S. Pat. No. 8,192,498 entitled “Posterior Cruciate-Retaining Orthopaedic Knee Prosthesis Having Controlled Condylar Curvature” by Christel M. Wagner, which was filed on Jun. 30, 2008; to U.S. Utility patent application Ser. No. 12/165,582, now U.S. Pat. No. 8,206,451 entitled “Posterior Stabilized Orthopaedic Prosthesis” by Joseph G. Wyss, which was filed on Jun. 30, 2008; and to U.S. Provisional Patent Application Ser. No. 61/077,124 entitled “Orthopaedic Knee Prosthesis Having Controlled Condylar Curvature” by Joseph G. Wyss, which was filed on Jun. 30, 2008; the entirety of each of which is incorporated herein by reference.


TECHNICAL FIELD

The present disclosure relates generally to orthopaedic prostheses, and particularly to orthopaedic prostheses for use in knee replacement surgery.


BACKGROUND

Joint arthroplasty is a well-known surgical procedure by which a diseased and/or damaged natural joint is replaced by a prosthetic joint. A typical knee prosthesis includes a tibial tray, a femoral component, and a polymer insert or bearing positioned between the tibial tray and the femoral component. Depending on the severity of the damage to the patient's joint, orthopaedic prostheses of varying mobility may be used. For example, the knee prosthesis may include a “fixed” tibial bearing in cases wherein it is desirable to limit the movement of the knee prosthesis, such as when significant soft tissue damage or loss is present. Alternatively, the knee prosthesis may include a “mobile” tibial bearing in cases wherein a greater degree of freedom of movement is desired. Additionally, the knee prosthesis may be a total knee prosthesis designed to replace the femoral-tibial interface of both condyles of the patient's femur or a uni-compartmental (or uni-condylar) knee prosthesis designed to replace the femoral-tibial interface of a single condyle of the patient's femur.


The type of orthopedic knee prosthesis used to replace a patient's natural knee may also depend on whether the patient's posterior cruciate ligament is retained or sacrificed (i.e., removed) during surgery. For example, if the patient's posterior cruciate ligament is damaged, diseased, and/or otherwise removed during surgery, a posterior stabilized knee prosthesis may be used to provide additional support and/or control at later degrees of flexion. Alternatively, if the posterior cruciate ligament is intact, a cruciate retaining knee prosthesis may be used.


Typical orthopaedic knee prostheses are generally designed to duplicate the natural movement of the patient's joint. As the knee is flexed and extended, the femoral and tibial components articulate and undergo combinations of relative anterior-posterior motion and relative internal-external rotation. However, the patient's surrounding soft tissue also impacts the kinematics and stability of the orthopaedic knee prosthesis throughout the joint's range of motion. That is, forces exerted on the orthopaedic components by the patient's soft tissue may cause unwanted or undesirable motion of the orthopaedic knee prosthesis. For example, the orthopaedic knee prosthesis may exhibit an amount of unnatural (paradoxical) anterior translation as the femoral component is moved through the range of flexion.


In a typical orthopaedic knee prosthesis, paradoxical anterior translation may occur at nearly any degree of flexion, but particularly at mid to late degrees of flexion. Paradoxical anterior translation can be generally defined as an abnormal relative movement of a femoral component on a tibial bearing wherein the contact “point” between the femoral component and the tibial bearing “slides” anteriorly with respect to the tibial bearing. This paradoxical anterior translation may result in loss of joint stability, accelerated wear, abnormal knee kinematics, and/or cause the patient to experience a sensation of instability during some activities.


SUMMARY

According to one aspect, a posterior stabilized orthopaedic knee prosthesis includes a femoral component and a tibial bearing. The femoral component may include a pair of spaced apart condyles defining an intracondylar notch therebetween. At least one of the pair of spaced apart condyles may have a condyle surface curved in the sagittal plane. The femoral component may also include a posterior cam positioned in the intracondylar notch. The tibial bearing may include a platform having a bearing surface configured to articulate with the condyle surface of the femoral component and a spine extending upwardly from the platform.


In some embodiments, the condyle surface of the femoral component may contact the bearing surface at a first contact point on the condyle surface at a first degree of flexion, contact the bearing surface at a second contact point on the condyle surface at a second degree of flexion, and contact the bearing surface at a third contact point on the condyle surface at a third degree of flexion. Additionally, the posterior cam of the femoral component may contact the spine of the tibial bearing at a fourth degree of flexion.


The second degree of flexion may be greater than the first degree of flexion and may be in the range of about 0 degrees to about 50 degrees in some embodiments. For example, in one embodiment, the second degree of flexion is no greater than about 30 degrees. The third degree of flexion may be greater than the second degree and less than about 90 degrees. For example, in one embodiment, the third degree of flexion is at least 30 degrees. In another embodiment, the third degree of flexion is at least 50 degrees. In still another embodiment, the third degree of flexion is at least 70 degrees. In some embodiments, the fourth degree of flexion is no greater than about 10 degrees more than the third degree of flexion. For example, in one particular embodiment, the fourth degree of flexion is no greater than the third degree of flexion. Additionally, in some embodiments, the fourth degree of flexion is at least 50 degrees. In another embodiment, the fourth degree of flexion is at least 70 degrees.


The condyle surface in the sagittal plane may have a first radius of curvature at the first contact point, a second radius of curvature at the second contact point, and a third radius of curvature at the third contact point. In some embodiments, the third radius of curvature is greater than the second radius of curvature by at least 0.5 millimeters. For example, the third radius of curvature may be greater than the second radius of curvature by at least 2 millimeters in some embodiments or 5 millimeters in other embodiments. Additionally, in some embodiments, the ratio of the second radius to the third radius is in the range of 0.75 to 0.85.


In some embodiments, the condyle surface of the femoral component in the sagittal plane may include first curved surface section and a second curved surface section. The first curved surface section may be defined between the first contact point and the second contact point. The second curved surface section may be defined between the second contact point and the third contact point. In such embodiments, the first curved surface section may have a substantially constant radius of curvature substantially equal to the second radius of curvature. Additionally, the second curved surface section may have a substantially constant radius of curvature substantially equal to the third radius of curvature.


According to another aspect, a posterior stabilized orthopaedic knee prosthesis includes a femoral component and a tibial bearing. The femoral component may include a pair of spaced apart condyles defining an intracondylar notch therebetween. At least one of the pair of spaced apart condyles may have a condyle surface curved in the sagittal plane. The femoral component may also include a posterior cam positioned in the intracondylar notch. The tibial bearing may include a platform having a bearing surface configured to articulate with the condyle surface of the femoral component and a spine extending upwardly from the platform.


In some embodiments, the condyle surface of the femoral component may contact the bearing surface at a first contact point on the condyle surface at a first degree of flexion. The first degree of flexion may be less than about 30 degrees. Additionally, the condyle surface may contact the bearing surface at a second contact point on the condyle surface at a second degree of flexion. The second degree of flexion may be in the range of 35 degrees to 90 degrees. The condyle surface of the femoral component may also contact the bearing surface at a third contact point on the condyle surface at a third degree of flexion. The third degree of flexion may be greater than the second degree of flexion. Additionally, the condyle surface may contact the bearing surface at a plurality of contact points between the first contact point and the second contact point when the femoral component is moved from the first degree of flexion to the second degree of flexion. Further, in some embodiments, the posterior cam of the femoral component may contact the spine of the tibial bearing at a fourth degree of flexion. The fourth degree of flexion at which the posterior cam contacts the spine may be less than, substantially equal to, or slightly greater than the third degree of flexion. For example, in one embodiment, the fourth degree of flexion is no greater than about 10 degrees more than the third degree of flexion.


In some embodiments, each contact point of the plurality of contact points is defined by a ray extending from a common origin to the respective contact point of the plurality of contact points. Each ray has a length defined by the following polynomial equation: rθ=(a+(b*θ)+(c*θ2)+(d*θ3)), wherein rθ is the length of the ray defining a contact point at θ degrees of flexion, a is a coefficient value between 20 and 50, and b is a coefficient value in a range selected from the group consisting of: −0.30<b<0.0, 0.00<b<0.30, and b=0. If b is in the range of −0.30<b<0.00, then c is a coefficient value between 0.00 and 0.012 and d is a coefficient value between −0.00015 and 0.00. Alternatively, if b is in the range of 0<b<0.30, then c is a coefficient value between −0.010 and 0.00 and d is a coefficient value between −0.00015 and 0.00. Alternatively still, if b is equal to 0, then c is a coefficient value in a range selected from the group consisting of: −0.0020<c<0.00 and 0.00<c<0.0025 and d is a coefficient value between −0.00015 and 0.00. In some embodiments, the distance between the origin of the first radius of curvature and the common origin of the rays is in the range of 0 and 10 millimeters.


In some embodiments, the first degree of flexion may be in the range of 0 degrees to 10 degrees, the second degree of flexion may be in the range of 45 degrees to 55 degrees, and the third degree of flexion may be in the range of about 65 degrees to about 75 degrees. For example, in one particular embodiment, the first degree of flexion is about 0 degrees, the second degree of flexion is about 50 degrees, and the third degree of flexion is about 70 degrees. Additionally, the fourth degree of flexion may be about 70 degrees.


In some embodiments, the condyle surface in the sagittal plane has a first radius of curvature at the first contact point, a second radius of curvature at the second contact point, and a third radius of curvature at the third radius of curvature. In such embodiments, the third radius of curvature is greater than the second radius of curvature by at least 0.5 millimeters. In some embodiments, the third radius of curvature may be greater than the first radius of curvature by at least 2 millimeters. Additionally, in some embodiments, the third radius of curvature is greater than the first radius of curvature by at least 5 millimeters.


Additionally, in some embodiments, the condyle surface of the femoral component in the sagittal plane may include a curved surface section defined between the second contact point and the third contact point. In such embodiments, the curved surface section may have a substantially constant radius of curvature substantially equal to the third radius of curvature.


According to yet another aspect, a posterior stabilized orthopaedic knee prosthesis may include a posterior stabilized orthopaedic knee prosthesis includes a femoral component and a tibial bearing. The femoral component may include a pair of spaced apart condyles defining an intracondylar notch therebetween. At least one of the pair of spaced apart condyles may have a condyle surface curved in the sagittal plane. The femoral component may also include a posterior cam positioned in the intracondylar notch. The tibial bearing may include a platform having a bearing surface configured to articulate with the condyle surface of the femoral component and a spine extending upwardly from the platform.


In some embodiments, the condyle surface of the femoral component may contact the bearing surface at a first contact point on the condyle surface at a first degree of flexion. The first degree of flexion may be less than about 30 degrees. Additionally, the condyle surface may contact the bearing surface at a second contact point on the condyle surface at a second degree of flexion. The second degree of flexion may be in the range of 35 degrees to 90 degrees. The condyle surface of the femoral component may also contact the bearing surface at a third contact point on the condyle surface at a third degree of flexion. The third degree of flexion may be greater than the second degree of flexion. In some embodiments, the posterior cam of the femoral component may contact the spine of the tibial bearing at a fourth degree of flexion. Additionally, the condyle surface may contact the bearing surface at a plurality of contact points between the first contact point and the second contact point when the femoral component is moved from the first degree of flexion to the second degree of flexion. Further, in some embodiments, the posterior cam of the femoral component may contact the spine of the tibial bearing at a fourth degree of flexion. The fourth degree of flexion may be equal to or less than the third degree of flexion.


In some embodiments, the condyle surface in the sagittal plane has a first radius of curvature at the first contact point, a second radius of curvature at the second contact point, and a third radius of curvature at the third radius of curvature. In such embodiments, the third radius of curvature is greater than the second radius of curvature by at least 2.0 millimeters.


Yet further, each contact point of the plurality of contact points may be defined by a ray extending from a common origin to the respective contact point of the plurality of contact points. Each ray has a length defined by the following polynomial equation: rθ=(a+(b*θ)+(c*θ2)+(d*θ3)), wherein rθ is the length of the ray defining a contact point at θ degrees of flexion, a is a coefficient value between 20 and 50, and b is a coefficient value in a range selected from the group consisting of: −0.30<b<0.0, 0.00<b<0.30, and b=0. If b is in the range of −0.30<b<0.00, then c is a coefficient value between 0.00 and 0.012 and d is a coefficient value between −0.00015 and 0.00. Alternatively, if b is in the range of 0<b<0.30, then c is a coefficient value between −0.010 and 0.00 and d is a coefficient value between −0.00015 and 0.00. Alternatively still, if b is equal to 0, then c is a coefficient value in a range selected from the group consisting of: −0.0020<c<0.00 and 0.00<c<0.0025 and d is a coefficient value between −0.00015 and 0.00. In some embodiments, the distance between the origin of the first radius of curvature and the common origin of the rays is in the range of 0 and 10 millimeters.


Additionally, in some embodiments, each of the pair of spaced apart condyles may include a condyle surface. In such embodiments, the condyle surfaces may be substantially symmetrical or may be asymmetrical.





BRIEF DESCRIPTION OF THE DRAWINGS

The detailed description particularly refers to the following figures, in which:



FIG. 1 is an exploded perspective view of one embodiment of an orthopaedic knee prosthesis;



FIG. 2 is a cross-sectional view of a femoral component and tibial bearing of FIG. 1 taken generally along section lines 2-2 and having the femoral component articulated to a first degree of flexion;



FIG. 3 is a cross-sectional view of a femoral component and tibial bearing of FIG. 2 having the femoral component articulated to a second degree of flexion;



FIG. 4 is a cross-sectional view of a femoral component and tibial bearing of FIG. 2 having the femoral component articulated to a third degree of flexion;



FIG. 5 is a cross-section view of one embodiment of the femoral component of FIG. 1;



FIG. 6 is a cross-section view of another embodiment of the femoral component of FIG. 1;



FIG. 7 is a cross-section view of another embodiment of the femoral component of FIG. 1;



FIG. 8 is a cross-section view of another embodiment of the femoral component of FIG. 1;



FIG. 9 is graph of the anterior-posterior translation of a simulated femoral component having an increased radius of curvature located at various degrees of flexion;



FIG. 10 is graph of the anterior-posterior translation of another simulated femoral component having an increased radius of curvature located at various degrees of flexion;



FIG. 11 is graph of the anterior-posterior translation of another simulated femoral component having an increased radius of curvature located at various degrees of flexion;



FIG. 12 is graph of the anterior-posterior translation of another simulated femoral component having an increased radius of curvature located at various degrees of flexion;



FIG. 13 is a cross-sectional view of another embodiment of the femoral component of FIG. 1;



FIG. 14 is a table of one embodiment of coefficient values of a polynomial equation defining the curve of the femoral component of FIG. 13 for a family of femoral component sizes;



FIG. 15 is a table of one embodiment of radii of curvature values and ratios for a family of femoral component sizes; and



FIG. 16 is a cross-section view of another condyle of another embodiment of the femoral component of FIG. 1.





DETAILED DESCRIPTION OF THE DRAWINGS

While the concepts of the present disclosure are susceptible to various modifications and alternative forms, specific exemplary embodiments thereof have been shown by way of example in the drawings and will herein be described in detail. It should be understood, however, that there is no intent to limit the concepts of the present disclosure to the particular forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.


Terms representing anatomical references, such as anterior, posterior, medial, lateral, superior, inferior, etcetera, may be used throughout this disclosure in reference to both the orthopaedic implants described herein and a patient's natural anatomy. Such terms have well-understood meanings in both the study of anatomy and the field of orthopaedics. Use of such anatomical reference terms in the specification and claims is intended to be consistent with their well-understood meanings unless noted otherwise.


Referring now to FIG. 1, in one embodiment, a posterior stabilized orthopaedic knee prosthesis 10 includes a femoral component 12, a tibial bearing 14, and a tibial tray 16. The femoral component 12 and the tibial tray 16 are illustratively formed from a metallic material such as cobalt-chromium or titanium, but may be formed from other materials, such as a ceramic material, a polymer material, a bio-engineered material, or the like, in other embodiments. The tibial bearing 14 is illustratively formed from a polymer material such as a ultra-high molecular weight polyethylene (UHMWPE), but may be formed from other materials, such as a ceramic material, a metallic material, a bio-engineered material, or the like, in other embodiments.


As discussed in more detail below, the femoral component 12 is configured to articulate with the tibial bearing 14, which is configured to be coupled with the tibial tray 16. The illustrative tibial bearing 14 is embodied as a rotating or mobile tibial bearing and is configured to rotate relative to the tibial tray 12 during use. However, in other embodiments, the tibial bearing 14 may be embodied as a fixed tibial bearing, which may be limited or restricted from rotating relative the tibial tray 16.


The tibial tray 16 is configured to be secured to a surgically-prepared proximal end of a patient's tibia (not shown). The tibial tray 16 may be secured to the patient's tibia via use of bone adhesive or other attachment means. The tibial tray 16 includes a platform 18 having an top surface 20 and a bottom surface 22. Illustratively, the top surface 20 is generally planar and, in some embodiments, may be highly polished. The tibial tray 16 also includes a stem 24 extending downwardly from the bottom surface 22 of the platform 18. A cavity or bore 26 is defined in the top surface 20 of the platform 18 and extends downwardly into the stem 24. The bore 26 is formed to receive a complimentary stem of the tibial insert 14 as discussed in more detail below.


As discussed above, the tibial bearing 14 is configured to be coupled with the tibial tray 16. The tibial bearing 14 includes a platform 30 having an upper bearing surface 32 and a bottom surface 34. In the illustrative embodiment wherein the tibial bearing 14 is embodied as a rotating or mobile tibial bearing, the bearing 14 includes a stem 36 extending downwardly from the bottom surface 32 of the platform 30. When the tibial bearing 14 is coupled to the tibial tray 16, the stem 36 is received in the bore 26 of the tibial tray 16. In use, the tibial bearing 14 is configured to rotate about an axis defined by the stem 36 relative to the tibial tray 16. In embodiments wherein the tibial bearing 14 is embodied as a fixed tibial bearing, the bearing 14 may or may not include the stem 36 and/or may include other devices or features to secure the tibial bearing 14 to the tibial tray 18 in a non-rotating configuration.


The upper bearing surface 32 of the tibial bearing 14 includes a medial bearing surface 42, a lateral bearing surface 44, and a spine 60 extending upwardly from the platform 16. The medial and lateral bearing surfaces 42, 44 are configured to receive or otherwise contact corresponding medial and lateral condyles 52, 54 of the femoral component 14 as discussed in more detail below. As such, each of the bearing surface 42, 44 has a concave contour. The spine 60 is positioned between the bearing surfaces 42, 44 and includes an anterior side 62 and a posterior side 64 having a cam surface 66. In the illustrative embodiment, the cam surface 66 has a substantially concave curvature. However, spines 60 including cam surfaces 66 having other geometries may be used in other embodiments. For example, a tibial bearing including a spine having a substantially “S”-shaped cross-sectional profile, such as the tibial bearing described in U.S. patent application Ser. No. 13/527,758, entitled “Posterior Stabilized Orthopaedic Prosthesis” by Joseph G. Wyss, et al., which is hereby incorporated by reference, may be used in other embodiments.


The femoral component 12 is configured to be coupled to a surgically-prepared surface of the distal end of a patient's femur (not shown). The femoral component 12 may be secured to the patient's femur via use of bone adhesive or other attachment means. The femoral component 12 includes an outer, articulating surface 50 having a pair of medial and lateral condyles 52, 54. In use, the condyles 52, 54 replace the natural condyles of the patient's femur and are configured to articulate on the corresponding bearing surfaces 42, 44 of the platform 30 of the tibial bearing 14.


The condyles 52, 54 are spaced apart to define an intracondyle notch or recess 56 therebetween. A posterior cam 80 and an anterior cam 82 (see FIG. 2) are positioned in the intracondyle notch 56. The posterior cam 80 is located toward the posterior side of the femoral component 12 and includes a cam surface 86 is configured to engage or otherwise contact the cam surface 66 of the spine 60 of the tibial bearing 12 during flexion as illustrated in and described in more detail below in regard to FIGS. 2-4.


It should be appreciated that the illustrative orthopaedic knee prosthesis 10 is configured to replace a patient's right knee and, as such, the bearing surface 42 and the condyle 52 are referred to as being medially located; and the bearing surface 44 and the condyle 54 are referred to as being laterally located. However, in other embodiments, the orthopaedic knee prosthesis 10 may be configured to replace a patient's left knee. In such embodiments, it should be appreciated that the bearing surface 42 and the condyle 52 may be laterally located and the bearing surface 44 and the condyle 54 may be medially located. Regardless, the features and concepts described herein may be incorporated in an orthopaedic knee prosthesis configured to replace either knee joint of a patient.


Referring now to FIGS. 2-4, the femoral component 12 is configured to articulate on the tibial bearing 14 during use. Each condyle 52, 54 of the femoral component 12 includes a condyle surface 100, which is convexly curved in the sagittal plane and configured to contact the respective bearing surface 42, 44. Additionally, during a predetermined range of flexion, the posterior cam 80 of the femoral component 12 contacts the spine 60 of the tibial bearing 14. For example, in one embodiment as shown in FIG. 2, when the orthopaedic knee prosthesis 10 is in extension or is otherwise not in flexion (e.g., a flexion of about 0 degrees), the condyle surface 100 of the condyle 52 contacts the bearing surface 42 (or bearing surface 44 in regard to condyle 54) at one or more contact points 100 on the condyle surface 100. Additionally, at this particular degree of flexion, the posterior cam 80 is not in contact with the spine 60. However, at later (i.e., larger) degrees of flexion, the posterior cam 80 is configured to contact the spine 60 to provide an amount of control over the kinematics of the orthopaedic prosthesis.


As the orthopaedic knee prosthesis 10 is articulated through the middle degrees of flexion, the femoral component 12 contacts the tibial bearing 14 at one or more contact points on the condyle surface 100. For example, in one embodiment as illustrated in FIG. 3, when the orthopaedic knee prosthesis 10 is articulated to a middle degree of flexion (e.g., at about 45 degrees), the condyle surface 100 contacts the bearing surface 42 at one or more contact points 104 on the condyle surface 100. As discussed in more detail below, depending on the particular embodiment, the posterior cam 80 may or may not be in contact with the spine 60 at this particular degree of flexion. Regardless, as the orthopaedic knee prosthesis 10 is articulated to a late degree of flexion (e.g., at about 70 degrees of flexion), the condyle surface 100 contacts the bearing surface 42 at one or more contact points 106 on the condyle surface 100 as illustrated in FIG. 4. Additionally, the posterior cam 80 is now in contact with the spine 60. It should be appreciated, of course, that the femoral component 12 may contact the tibial bearing 14 at a plurality of contact points on the condyle surface 100 at any one particular degree of flexion. However, for clarity of description, only the contact points 102, 104, 106 have been illustrated in FIGS. 2-4, respectively.


The particular degree of flexion at which the posterior cam 80 initially contacts the spine 60 is based on the particular geometry of the condyle surface 100 of the femoral component 12. For example, in the illustrative embodiment of FIGS. 2-4, the orthopaedic knee prosthesis 10 is configured such that the posterior cam 80 initially contacts the spine 60 at about 70 degrees of flexion. However, in other embodiments the posterior cam 80 may initially contact the spine 60 at other degrees of flexion as discussed in more detail below.


The orthopaedic knee prosthesis 10 is configured such that the amount of paradoxical anterior translation of the femoral component 12 relative to the tibial bearing 14 may be reduced or otherwise delayed to a later (i.e., larger) degree of flexion. In particular, as discussed in more detail below, the condyle surface 100 of one or both of the condyles 52, 54 has particular geometry or curvature configured to reduce and/or delay anterior translations and, in some embodiments, promote “roll-back”or posterior translation, of the femoral component 12. It should be appreciated that by delaying the onset of paradoxical anterior translation of the femoral component 12 to a larger degree of flexion, the overall occurrence of paradoxical anterior translation may be reduced during those activities of a patient in which deep flexion is not typically obtained.


In a typical orthopaedic knee prosthesis, paradoxical anterior translation may occur whenever the knee prosthesis is positioned at a degree of flexion greater than zero degrees. The likelihood of anterior translation generally increases as the orthopaedic knee prosthesis is articulated to larger degrees of flexion, particularly in the mid-flexion range. In such orientations, paradoxical anterior translation of the femoral component on the tibial bearing can occur whenever the tangential (traction) force between the femoral component and the tibial bearing fails to satisfy the following equation:

T<μN  (1)


wherein “T” is the tangential (traction) force, “μ” is the coefficient of friction of the femoral component and the tibial bearing, and “N” is the normal force between the femoral component and the tibial bearing. As a generalization, the tangential (traction) force between the femoral component and the tibial bearing can be defined as

T=M/R  (2)


wherein “T” is the tangential (traction) force between the femoral component and the tibial bearing, “M” is the knee moment, and “R” is the radius of curvature in the sagittal plane of the condyle surface in contact with the tibial bearing at the particular degree of flexion. It should be appreciated that equation (2) is a simplification of the governing real-world equations, which does not consider such other factors as inertia and acceleration. Regardless, the equation (2) provides insight that paradoxical anterior translation of an orthopaedic knee prosthesis may be reduced or delayed by controlling the radius of curvature of the condyle surface of the femoral component. That is, by controlling the radius of curvature of the condyle surface (e.g., increasing or maintaining the radius of curvature), the right-hand side of equation (2) may be reduced, thereby decreasing the value of the tangential (traction) force and satisfying the equation (1). As discussed above, by ensuring that the tangential (traction) force satisfies equation (1), paradoxical anterior translation of the femoral component on the tibial bearing may be reduced or otherwise delayed to a greater degree of flexion.


Based on the above analysis, to reduce or delay the onset of paradoxical anterior translation, the geometry of the condyle surface 100 of one or both of the condyles 52, 54 of the femoral component 12 is controlled. For example, in some embodiments, the radius of curvature of the condyle surface 100 is controlled such that the radius of curvature is held constant over a range of degrees of flexion and/or is increased in the early to mid flexion ranges. Comparatively, typical femoral components have decreasing radii of curvatures beginning at the distal radius of curvature (i.e., at about 0 degrees of flexion). However, it has been determined that by maintaining a relatively constant radius of curvature (i.e., not decreasing the radius of curvature) over a predetermined range of degrees of early to mid-flexion and/or increasing the radius of curvature over the predetermined range of degrees of flexion may reduce or delay paradoxical anterior translation of the femoral component 12.


Additionally, in some embodiments, the condyle surface 100 is configured or designed such that the transition between discrete radii of curvature of the condyle surface 100 is gradual. That is, by gradually transitioning between the discrete radii of curvature, rather than abrupt transitions, paradoxical anterior translation of the femoral component 12 may be reduced or delayed. Further, in some embodiments, the rate of change in the radius of curvature of the condyle surface in the early to mid flexion ranges (e.g., from about 0 degrees to about 90 degrees) is controlled such that the rate of change is less than a predetermined threshold. That is, it has been determined that if the rate of change of the radius of curvature of the condyle surface 100 is greater than the predetermined threshold, paradoxical anterior translation may occur.


Accordingly, in some embodiments as illustrated in FIGS. 5-8, the condyle surface 100 of the femoral component 12 has an increased radius of curvature in early to middle degrees of flexion. By increasing the radius of curvature, paradoxical anterior translation may be reduced or delayed to a later degree of flexion as discussed in more detail below. In particular, paradoxical anterior translation may be delayed to a degree of flexion at or beyond which the posterior cam 80 of the femoral component 12 initially contacts the spine 60 of the tibial bearing 14. Once the posterior cam 80 is in contact with the spine 60, paradoxical anterior translation is controlled by the engagement of the posterior cam 80 to the spine 60. That is, the posterior cam 80 may be restricted from moving anteriorly by the spine 60.


The amount of increase between the radius of curvature R2 and the radius of curvature R3, as well as, the degree of flexion on the condyle surface 100 at which such increase occurs has been determined to affect the occurrence of paradoxical anterior translation. As discussed in more detail in the U.S. patent application Ser. No. 12/165,579, now U.S. Pat. No. 8,828,086, entitled “Orthopaedic Femoral Prosthesis Having Controlled Condylar Curvature”, which was filed concurrently herewith and is hereby incorporated by reference, multiple simulations of various femoral component designs were performed using the LifeMOD/Knee Sim, version 1007.1.0 Beta 16 software program, which is commercially available from LifeModeler, Inc. of San Clemente, Calif., to analyze the effect of increasing the radius of curvature of the condyle surface of the femoral components in early and mid flexion. Based on such analysis, it has been determined that paradoxical anterior translation of the femoral component relative to the tibial bearing may be reduced or otherwise delayed by increasing the radius of curvature of the condyle surface by an amount in the range of about 0.5 millimeters to about 5 millimeters or more at a degree of flexion in the range of about 30 degrees of flexion to about 90 degrees of flexion.


For example, the graph 200 illustrated in FIG. 9 presents the results of a deep bending knee simulation using a femoral component wherein the radius of curvature of the condyle surface is increased by 0.5 millimeters (i.e., from 25.0 millimeters to 25.5 millimeters) at 30 degrees of flexion, at 50 degrees of flexion, at 70 degrees of flexion, and at 90 degrees of flexion. Similarly, the graph 300 illustrated in FIG. 10 presents the results of a deep bending knee simulation using a femoral component wherein the radius of curvature of the condyle surface is increased by 1.0 millimeters (i.e., from 25.0 millimeters to 26.0 millimeters) at 30 degrees of flexion, at 50 degrees of flexion, at 70 degrees of flexion, and at 90 degrees of flexion. The graph 400 illustrated in FIG. 11 presents the results of a deep bending knee simulation using a femoral component wherein the radius of curvature of the condyle surface is increased by 2.0 millimeters (i.e., from 25.0 millimeters to 27.0 millimeters) at 30 degrees of flexion, at 50 degrees of flexion, at 70 degrees of flexion, and at 90 degrees of flexion. Additionally, the graph 500 illustrated in FIG. 12 presents the results of a deep bending knee simulation using a femoral component wherein the radius of curvature of the condyle surface is increased by 5.0 millimeters (i.e., from 25.0 millimeters to 26.0 millimeters) at 30 degrees of flexion, at 50 degrees of flexion, at 70 degrees of flexion, and at 90 degrees of flexion.


In the graphs 200, 300, 400, 500, the condylar lowest or most distal points (CLP) of the medial condyle (“med”) and the lateral condyle (“lat”) of the femoral component are graphed as a representation of the relative positioning of the femoral component to the tibial bearing. As such, a downwardly sloped line represents roll-back of the femoral component on the tibial bearing and an upwardly sloped line represents anterior translation of the femoral component on the tibial bearing.


As illustrated in the graphs 200, 300, 400, 500, anterior sliding of the femoral component was delayed until after about 100 degrees of flexion in each of the embodiments; and the amount of anterior translation was limited to less than about 1 millimeter. In particular, “roll-back” of the femoral component on the tibial bearing was promoted by larger increases in the radius of curvature of the condyle surface at earlier degrees of flexion. Of course, amount of increase in the radius of curvature and the degree of flexion at which such increase is introduced is limited by other factors such as the anatomical joint space of the patient's knee, the size of the tibial bearing, and the like. Regardless, based on the simulations reported in the graphs 200, 300, 400, 500, paradoxical anterior translation of the femoral component on the tibial bearing can be reduced or otherwise delayed by increasing the radius of curvature of the condyle surface of the femoral component during early to mid flexion.


Accordingly, referring back to FIGS. 5-8, the condyle surface 100 in the sagittal plane is formed in part from a number of curved surface sections 102, 104, 106, 108 the sagittal ends of each of which are tangent to the sagittal ends of any adjacent curved surface section of the condyles surface 100. Each curved surface section 102, 104, 106, 108 is defined by a radius of curvature. In particular, the curved surface section 102 is defined by a radius of curvature R2, the curved surface section 104 is defined by a radius of curvature R3, the curved surface section 106 is defined by a radius of curvature R4.


The condyle surface 100 of the femoral component 12 is configured such that the radius of curvature R3 of the curved surface section 104 is greater than the radius of curvature R2 of the curved surface section 102. In one embodiment, the radius of curvature R3 is greater than the radius of curvature R2 by 0.5 millimeters or more. In another embodiment, the radius of curvature R3 is greater than the radius of curvature R2 by 2 millimeters or more. In another embodiment, the radius of curvature R3 is greater than the radius of curvature R2 by 2 millimeters or more. In a particular embodiment, the radius of curvature R3 is greater than the radius of curvature R2 by at least 5 millimeters or more. It should be appreciated, however, that the particular increase of radius of curvature between R2 and R3 may be based on or scaled to the particular size of the femoral component 12 in some embodiments.


Each of the curved surface sections 102, 104, 106, 108 contacts the bearing surface 42 (or 44) of the tibial bearing 14 through different ranges of degrees of flexion. For example, the curved surface section 102 extends from an earlier degree of flexion θ1 to a later degree of flexion θ2. The curved surface section 104 extends from the degree of flexion θ2 to a later degree of flexion θ3. The curved surface section 106 extends from the degree of flexion θ3 to a later degree of flexion θ4.


For example, in one embodiment, as illustrated in FIG. 5, the curved surface section 102 extends from a degree of flexion θ1 of about 0 degrees of flexion to a degree of flexion θ2 of about 50 degrees of flexion. The curved surface section 104 extends from the degree of flexion θ2 of about 50 degrees of flexion to a degree of flexion θ3 of about 70 degrees of flexion. The curved surface section 106 extends from the degree of flexion θ3 of about 70 degrees of flexion to a degree of flexion θ4 of about 120 degrees of flexion. In the illustrative embodiment of FIG. 5, the posterior cam 80 of the femoral component 12 is configured to engage or contact the spine 60 of the tibial bearing 14 at a degree of flexion θC of about 70 degrees of flexion. However, in other embodiments, the posterior cam 80 may be configured to engage the spine 60 at a degree of flexion earlier or later than 70 degrees. By ensuring the posterior cam 80 engages or contacts the spine 60 prior to or soon after the reduction in radius of curvature from R3 to R4, the control of the kinematics of the orthopaedic prosthesis can be transitioned from the geometry of the condyle surface 100 to the interaction of the posterior cam 80 and spine 60, which may further reduce the amount of anterior translation of the femoral component 12. For example, in one particular embodiment, the posterior cam 80 may be configured to engage or contact the spine 60 at a degree of flexion θC that is no greater than 10 degrees more than the degree of flexion θ3 at which the radius curvature of the condyle surface 100 decreases from the radius of curvature R3 to the radius of curvature R4.


In another embodiment, as illustrated in FIG. 6, the curved surface section 102 extends from a degree of flexion θ1 of about 0 degrees of flexion to a degree of flexion θ2 of about 10 degrees of flexion. The curved surface section 104 extends from the degree of flexion θ2 of about 10 degrees of flexion to a degree of flexion θ3 of about 30 degrees of flexion. The curved surface section 106 extends from the degree of flexion θ3 of about 30 degrees of flexion to a degree of flexion θ4 of about 120 degrees of flexion. In the illustrative embodiment of FIG. 6, the posterior cam 80 of the femoral component 12 is configured to engage or contact the spine 60 of the tibial bearing 14 at a degree of flexion θC of about 30 degrees of flexion. Again, however, the posterior cam 80 may be configured to engage the spine 60 at a degree of flexion earlier than 30 degrees (i.e., earlier than the reduction in radius of curvature from R3 to R4) or soon thereafter (e.g., within 0-10 degrees) in other embodiments.


In another embodiment, as illustrated in FIG. 7, the curved surface section 102 extends from a degree of flexion θ1 of about 0 degrees of flexion to a degree of flexion θ2 of about 30 degrees of flexion. The curved surface section 104 extends from the degree of flexion θ2 of about 30 degrees of flexion to a degree of flexion θ3 of about 50 degrees of flexion. The curved surface section 106 extends from the degree of flexion θ3 of about 50 degrees of flexion to a degree of flexion θ4 of about 120 degrees of flexion. In the illustrative embodiment of FIG. 7, the posterior cam 80 of the femoral component 12 is configured to engage or contact the spine 60 of the tibial bearing 14 at a degree of flexion θC of about 50 degrees of flexion. Again, however, the posterior cam 80 may be configured to engage the spine 60 at a degree of flexion earlier than 50 degrees (i.e., earlier than the reduction in radius of curvature from R3 to R4) or soon thereafter (e.g., within 0-10 degrees) in other embodiments.


In another embodiment, as illustrated in FIG. 8, the curved surface section 102 extends from a degree of flexion θ1 of about 0 degrees of flexion to a degree of flexion θ2 of about 70 degrees of flexion. The curved surface section 104 extends from the degree of flexion θ2 of about 70 degrees of flexion to a degree of flexion θ3 of about 90 degrees of flexion. The curved surface section 106 extends from the degree of flexion θ3 of about 90 degrees of flexion to a degree of flexion θ4 of about 120 degrees of flexion. In the illustrative embodiment of FIG. 8, the posterior cam 80 of the femoral component 12 is configured to engage or contact the spine 60 of the tibial bearing 14 at a degree of flexion θC of about 90 degrees of flexion. Again, however, the posterior cam 80 may be configured to engage the spine 60 at a degree of flexion earlier than 90 degrees (i.e., earlier than the reduction in radius of curvature from R3 to R4) or soon thereafter (e.g., within 0-10 degrees) in other embodiments.


It should be appreciated that the embodiments of FIGS. 5-8 are illustrative embodiments and, in other embodiments, each of the curved surface sections 102, 104, 106 may extend from degrees of flexion different from those shown and discussed above in regard to FIGS. 5-8. For example, in each of the embodiments of FIGS. 5-8, although the curved surface section 102 is illustrated as beginning at about 0 degrees of flexion, the curved surface section 102 may being at a degree of flexion prior to 0 degrees of flexion (i.e., a degree of hyperextension) in other embodiments.


Additionally, it should be appreciated that the degree of flexion θC at which the posterior cam 80 contacts the spine 60 may be less than, substantially equal to, or slightly greater than the degree of flexion θ3 at which the radius of curvature R3 decreases to the radius of curvature R4. In some embodiments, the degree of flexion θC is within a predetermined threshold of the degree of flexion θ3. For example, in one particular embodiment, the degree of flexion θC is within about 10 degrees of the degree of flexion θ3. For example, the radius of curvature R3 may decrease to the radius of curvature R4 at a degree of flexion θ3 of about 70 degrees and the posterior cam 80 may be configured to initially contact the spine 60 at a degree of flexion θC of in the range of about 60 to about 80 degrees of flexion.


Referring now to FIGS. 13-15, in some embodiments, the condyle surface 100 includes a gradual transition between discreet radii of curvature in the early to mid flexion ranges such that the change in the radius of curvature of the condyle surface over a range of degrees of flexion is reduced. For example, as illustrated in FIG. 13, the curved surface section 102 in some embodiments is designed to provide a gradual transition from the first radius of curvature R1 to the second radius of curvature R2. To do so, the curved surface section 102 is defined by a plurality of rays 120 rather than a constant radius of curvature as illustrated in and described above in regard to FIGS. 5-8. Each of the plurality of rays 120 originate from a common origin O. Additionally, each of the plurality of rays 120 defines a respective contact point 130 on the curved surface section 120. Although only three rays 120 are illustrated in FIG. 13 for clarity of the drawing, it should be appreciated that an infinite number of rays 120 may be used to define the curved surface section 102.


The location of each contact points 130, which collectively define the curved surface section 102, can be determined based on the length of each ray 120 at each degree of flexion. In particular and unexpectedly, it has been determined that paradoxical anterior translation of the femoral component 12 on the tibial bearing 14 may be reduced or delayed by defining the curved surface section 102 according to the following polynomial equation:

rθ=(a+(b*θ)+(c*θ2)+(d*θ3)),  (3)


wherein “rθ” is the length of a ray 120 (in metric units) defining a contact point 130 on the curved surface section 104 at “θ” degrees of flexion, “a” is a scalar value between 20 and 50, and “b” is a coefficient value selected such that:

−0.30<b<0.00,
0.00<b<0.30, or
b=0  (4)


If the selected coefficient “b” is in the range of −0.30<b<0.00, then coefficients “c” and “d” are selected such that:

0.00<c<0.012, and
−0.00015<d<0.00.  (5)


Alternatively, if the selected coefficient “b” is in the range of 0.00<b<0.30, then coefficients “c” and “d” are selected such that:

−0.010<c<0.00, and
−0.00015<d<0.00.  (6)


Further, if the selected coefficient “b” is equal to 0, then coefficients “c” and “d” are selected such that:

−0.0020<c<0.00, or
0.00<c<0.0025, and
−0.00015<d<0.00.  (7)


It should be appreciated that ranges of values for the scalar “a” and coefficients “b”, “c”, and “d” have been determined from an infinite number of possible solutions for the polynomial equation (3). That is, the particular set of ranges provided above have been determined to generate a family of curves (i.e., the curved surface section 102) that provide a gradual transitioning of the condyle surface 100 from the radius of curvature R1 to the radius of curvature R2 such that anterior translation of the femoral component 12 relative to the tibial bearing 14 is reduced or delayed. Additionally, it should be appreciated that the range of values for each coefficient “a”, “b”, “c”, and “d” are provided above in regard to embodiments designed using the metric system of units. However, such range of coefficient values may be converted for use in embodiments using other systems of units such as the English system of units.


The overall shape of the curved surface section 102 is also affected by the placement of the common origin O of the plurality of rays 120. By limiting the distance 124 between the common origin O of the plurality of rays 120 and the origin 122 of the distal radius of curvature R1, paradoxical anterior sliding of the femoral component 12 on the tibial bearing 14 may be reduced or delayed. Additionally, stability of the orthopaedic knee prosthesis 10 may be improved by ensuring the common origin O of the plurality of rays 120 is within the predetermined distance 124 from the origin 122 of the distal radius of curvature R1. As such, in one embodiment, the location of the common origin O of the plurality of rays 120 is selected such that the distance 124 between the common origin O and the origin 120 of the radius of curvature R1 is less than about 10 millimeters to reduce or delay anterior translation of the femoral component and/or provide improved stability to the orthopaedic knee prosthesis 10.


It should be appreciated that the distance 124 between the common origin O and the origin 122 of the radius of curvature R1 and the particular coefficient values may be dependent upon the particular size of the femoral component 12 in some embodiments. For example, as illustrated in FIG. 14, a table 700 illustrates one particular embodiment of coefficient values for the above-defined polynomial equation (3) and values for the distance 124 defined between the common origin O and the origin 122 of the distal radius of curvature R1. As shown in table 700, the distance 124 between the common origin O and the origin 122 of the radius of curvature R1 and the value for the scalar “a” change across the femoral component sizes. However, in this particular embodiment, the values for the coefficients “b”, “c”, and “d” are constant across the femoral component sizes. It should be appreciated, however, that in other embodiments, the coefficient values “b”, “c”, and “d” may change across the femoral component sizes.


As discussed above, in some embodiments, the condyle surface 100 is further designed or configured such that the change in the radius of curvature of the condyle surface 100 in the early and mid flexion ranges is not too great or too abrupt (e.g., the ratio of the degree of change in radius of curvature to the change in degrees of flexion is too great). That is, if the ratio of the radius of curvature R1 to the radius of curvature R2, R3, or R4 is too great, paradoxical anterior translation of the femoral component 12 may occur. As such, by designing the condyle surface 100 of the femoral component 12 such that the ratios of the distal radius of curvature R1 to (i) the radius of curvature R2 of the curved surface section 102, (ii) the radius of curvature R3 of the curved surface section 104, and (iii) the radius of curvature R4 of the late flexion curved surface section 106 are less than a predetermined threshold value, paradoxical anterior sliding may unexpectedly be reduced or otherwise delayed.


Accordingly, in one particular embodiment, the condyle surface 100 of the femoral component 12 is designed such that the ratio of the radius of curvature of R1 to the radius of curvature of R2 is between about 1.10 to about 1.30, the ratio of the radius of curvature of R1 to the radius of curvature R3 is between about 1.001 to about 1.100, and the ratio of the radius of curvature of R1 to the radius of curvature R4 is about 1.25 to about 2.50. Further, in some embodiments, the ratio of the radius of curvature of R2 to the radius of curvature of R3 is between about 0.74 and about 0.85.


It should be appreciated that the particular amount of increase in the radius of curvature R2 to R3 of the condyle surface 100 of the femoral component 12 and/or the positioning of such increase on the condyle surface 100 may also be based on, scaled, or otherwise affected by the size of the femoral component 12. That is, it should be appreciated that an increase of the radius of curvature R2 to R3 of the condyle surface 100 of 0.5 millimeters is a relatively larger increase in small-sized femoral components compared to larger-sized femoral components. As such, the magnitude of the increase in the radius of curvature R2 to R3 of the condyle surface 100 of the femoral component 12 may change across femoral component sizes. In one embodiment, however, the ratios of the radius of curvatures R1 to the radius of curvatures R2, R3, and R4 are maintained at a substantially constant value across the family of femoral component sizes.


For example, as illustrated in FIG. 15, a table 800 defines the length of each radius of curvature R1, R2, R3, R4 for a family of femoral component sizes 1 through 10. As illustrated in the table 850, the length of each radius of curvature R1, R2, R3, R4 for each size 1-10 of the femoral component 12 is selected such that the ratios of R1/R2 and R1/R3 are substantially constant across the femoral component sizes. In the illustrative embodiment, as previously discussed, the ratio of the radius of curvature R1 to the radius of curvature R2 is maintained at a value of about 1.25 to about 1.27 across the femoral component sizes 1 through 10 and the ratio of the radius of curvature R1 to the radius of curvature R3 is maintained at a value of about 1.005 across the femoral component sizes 1 through 10.


The overall shape and design of the condyle surface 100 of the femoral component 12 has been described above in regard to a single condyle 52, 54 of the femoral component 12. It should be appreciated that in some embodiments both condyles 52, 54 of the femoral component 12 may be symmetrical and have similar condyle surfaces 100. However, in other embodiments, the condyles 52, 54 of the femoral component 12 may be asymmetrical. For example, as illustrated in FIG. 16, the femoral component 12 may include a second condyle 52, 54 having a condyle surface 300, which is defined in part by a plurality of curved surface sections 302, 304, 306. The curved surface section 302 extends from an earlier degree of flexion θ5 to a later degree of flexion θ6. The curved surface section 304 extends from the degree of flexion θ6 to a later degree of flexion θ7. The curved surface section 306 extends from the degree of flexion θ7 to a later degree of flexion θ8. The condyle surface 300 also includes a distal radius R5, which is gradually transitioned to a radius of curvature R6 via the curved surface section 302. Additionally, the curved section 304 is defined by a radius of curvature R7 and the curved section 306 is defined by a radius of curvature R8.


As such, in embodiments wherein the condyles 52, 54 are symmetrical, the degree of flexion θ5 is substantially equal to the degree of flexion θ1, the degree of flexion θ6 is substantially equal to the degree of flexion θ2, the degree of flexion θ7 is substantially equal to the degree of flexion θ3, and the degree of flexion θ8 is substantially equal to the degree of flexion θ4. Additionally, the radius of curvature R5 is substantially equal to the radius of curvature R1, the radius of curvature R6 is substantially equal to the radius of curvature R2, the radius of curvature R7 is substantially equal to the radius of curvature R3, and the radius of curvature R8 is substantially equal to the radius of curvature R4. Further, the set of coefficient values “a”, “b”, “c”, and/or “d” of the equation (4) described above are substantially similar for both condyles.


However, in other embodiments, the condyles 52, 54 are asymmetrical. As such, the degree of flexion θ5 may be different from the degree of flexion θ1. Additionally, the degree of flexion θ6 may be different from the degree of flexion θ2. That is, the increase in radius of curvature between R2 and R3 may occur at different degrees of flexion between the condyles 52, 54. Further, the degree of flexion θ8 may be different from the degree of flexion θ4. It should be appreciated, however, that the degree of flexion θ7 may be substantially equal to the degree of flexion θ3 such that the posterior cam 80 is positioned properly within the intracondylar notch 56.


Additionally, in those embodiments wherein the condyles 52, 54 are asymmetrical, the radius of curvature R5 may be different from the radius of curvature R1, the radius of curvature R6 may be different from the radius of curvature R2, the radius of curvature R7 may be different from the radius of curvature R3, and/or the radius of curvature R8 may be different from the radius of curvature R4. Further, the set of coefficient values “a”, “b”, “c”, and/or “d” of the equation (3) described above may be different between the condyle surfaces 100 and 300.


While the disclosure has been illustrated and described in detail in the drawings and foregoing description, such an illustration and description is to be considered as exemplary and not restrictive in character, it being understood that only illustrative embodiments have been shown and described and that all changes and modifications that come within the spirit of the disclosure are desired to be protected.


There are a plurality of advantages of the present disclosure arising from the various features of the devices and assemblies described herein. It will be noted that alternative embodiments of the devices and assemblies of the present disclosure may not include all of the features described yet still benefit from at least some of the advantages of such features. Those of ordinary skill in the art may readily devise their own implementations of the devices and assemblies that incorporate one or more of the features of the present invention and fall within the spirit and scope of the present disclosure as defined by the appended claims.

Claims
  • 1. An orthopaedic knee prosthesis comprising: a femoral component having a medial condyle surface curved in the sagittal plane and a lateral condyle surface curved in the sagittal plane; anda tibial bearing having a medial bearing surface corresponding to and configured to articulate with the medial condyle surface of the femoral component and a lateral bearing surface corresponding to and configured to articulate with the lateral condyle surface of the femoral component,wherein the medial condyle surface (i) contacts the medial bearing surface at a first contact point on the medial condyle surface at a first degree of flexion, the first degree of flexion being less than 30 degrees, and (ii) contacts the medial bearing surface at a second contact point on the medial condyle surface at a second degree of flexion, the second degree of flexion being greater than the first degree of flexion,wherein the lateral condyle surface (i) contacts the lateral bearing surface at a first contact point on the lateral condyle surface at a third degree of flexion, the third degree of flexion being less than 30 degrees and the third degree of flexion being different from the first degree of flexion, and (ii) contacts the lateral bearing surface at a second contact point on the lateral condyle surface at a fourth degree of flexion, the fourth degree of flexion being greater than the third degree of flexion,wherein the medial condyle surface is shaped such that in the sagittal plane the medial condyle surface (i) has a first radius of curvature at the first contact point on the medial condyle surface, and (ii) has a second radius of curvature at the second contact point on the medial condyle surface different from the first radius of curvature, andwherein the lateral condyle surface is shaped such that in the sagittal plane the lateral condyle surface (i) has a third radius of curvature at the first contact point on the lateral condyle surface, the third radius of curvature being different than the first radius of curvature, and (ii) has a fourth radius of curvature at the second contact point on the lateral condyle surface, the fourth radius of curvature being different from the second radius of curvature and the third radius of curvature,wherein the medial condyle surface has a first plurality of radii of curvature between the first contact point and the second contact point on the medial condyle surface to transition from the first radius of curvature to the second radius of curvature over a range of flexion,wherein the lateral condyle surface has a second plurality of radii of curvature between the first contact point and the second contact point on the lateral condyle surface to transition from the third radius of curvature to the fourth radius of curvature over a range of flexion,wherein the first degree of flexion is in the range of 0 degrees to 10 degrees, and the second degree of flexion is in the range of 45 degrees to 55 degrees, andwherein a difference between the first radius of curvature and the second radius of curvature is different from a difference between the third radius of curvature and the fourth radius of curvature.
  • 2. The orthopaedic knee prosthesis of claim 1, wherein the third degree of flexion is in the range of 0 degrees to 10 degrees, and the fourth degree of flexion is in the range of 45 degrees to 55 degrees.
  • 3. The orthopaedic knee prosthesis of claim 1, wherein each of the third degree of flexion and the fourth degree of flexion is in the range of 0 degrees to 10 degrees.
  • 4. The orthopaedic knee prosthesis of claim 1, wherein the third degree of flexion is in the range of 0 degrees to 10 degrees, and the fourth degree of flexion is in the range of 25 degrees to 35 degrees.
  • 5. The orthopaedic knee prosthesis of claim 1, wherein the third degree of flexion is in the range of 0 degrees to 10 degrees, and the fourth degree of flexion is in the range of 65 degrees to 75 degrees.
  • 6. The orthopaedic knee prosthesis of claim 1, wherein the fourth degree of flexion is different from the second degree of flexion.
  • 7. The orthopaedic knee prosthesis of claim 1, wherein a first ratio of the first radius of curvature to the second radius of curvature is equal to a second ratio of the third radius of curvature to the fourth radius of curvature.
  • 8. The orthopaedic knee prosthesis of claim 1, wherein a ratio of the first radius of curvature to the second radius of curvature is between about 1.10 to about 1.30.
  • 9. The orthopaedic knee prosthesis of claim 8, wherein a ratio of the third radius of curvature to the fourth radius of curvature is between about 1.10 to about 1.30.
  • 10. The orthopaedic knee prosthesis of claim 1, wherein the first radius of curvature of the medial condyle surface has an origin, the first plurality of radii of curvature of the medial condyle surface have a common origin, and a distance between the origin of the first radius of curvature and the common origin of the first plurality of radii of curvature is in the range of 0 and 10 millimeters.
  • 11. The orthopaedic knee prosthesis of claim 1, wherein the third radius of curvature of the lateral condyle surface has an origin, the second plurality of radii of curvature of the lateral condyle surface have a common origin, and a distance between the origin of the third radius of curvature and the common origin of the second plurality of radii of curvature is in the range of 0 and 10 millimeters.
  • 12. The orthopaedic knee prosthesis of claim 1, wherein the distance between the origin of the first radius of curvature and the common origin of the first plurality of radii of curvature is different from the distance between the origin of the third radius of curvature and the common origin of the second plurality of radii of curvature.
  • 13. The orthopaedic knee prosthesis of claim 1, wherein: the medial condyle surface contacts the medial bearing surface at a third contact point on the medial condyle surface at a fifth degree of flexion greater than the second degree of flexion,the medial condyle surface in the sagittal plane has a fifth radius of curvature at the third contact point, andthe fifth radius of curvature is greater than the second radius of curvature by at least 0.5 millimeters.
  • 14. The orthopaedic knee prosthesis of claim 13, wherein: the lateral condyle surface contacts the medial bearing surface at a third contact point on the lateral condyle surface at a sixth degree of flexion greater than the fourth degree of flexion,the lateral condyle surface in the sagittal plane has a sixth radius of curvature at the third contact point, andthe sixth radius of curvature is greater than the fourth radius of curvature by at least 0.5 millimeters.
  • 15. An orthopaedic knee prosthesis comprising: a femoral component having (i) a medial condyle surface curved in the sagittal plane, (ii) a lateral condyle surface curved in the sagittal plane and spaced apart from the medial condyle surface to define an intracondylar notch therebetween, and (iii) a posterior cam positioned in the intercondylar notch; anda tibial bearing having (i) a medial bearing surface corresponding to and configured to articulate with the medial condyle surface of the femoral component, (ii) a lateral bearing surface corresponding to and configured to articulate with the lateral condyle surface of the femoral component, and (iii) a spine positioned between the medial bearing surface and the lateral bearing surface,wherein the medial condyle surface (i) contacts the medial bearing surface at a first contact point on the medial condyle surface at a first degree of flexion, the first degree of flexion being less than 30 degrees, and (ii) contacts the medial bearing surface at a second contact point on the medial condyle surface at a second degree of flexion, the second degree of flexion being greater than the first degree of flexion,wherein the lateral condyle surface (i) contacts the lateral bearing surface at a first contact point on the lateral condyle surface at a third degree of flexion, the third degree of flexion being less than 30 degrees and the third degree of flexion being different from the first degree of flexion, and (ii) contacts the lateral bearing surface at a second contact point on the lateral condyle surface at a fourth degree of flexion, the fourth degree of flexion being greater than the third degree of flexion,wherein the medial condyle surface is shaped such that in the sagittal plane the medial condyle surface (i) has a first radius of curvature at the first contact point on the medial condyle surface, and (ii) has a second radius of curvature at the second contact point on the medial condyle surface different from the first radius of curvature, andwherein the lateral condyle surface is shaped such that in the sagittal plane the lateral condyle surface (i) has a third radius of curvature at the first contact point on the lateral condyle surface, the third radius of curvature being different than the first radius of curvature, and (ii) has a fourth radius of curvature at the second contact point on the lateral condyle surface, the fourth radius of curvature being different from the second radius of curvature and the third radius of curvature,wherein the medial condyle surface has a first plurality of radii of curvature between the first contact point and the second contact point on the medial condyle surface to transition from the first radius of curvature to the second radius of curvature over a range of flexion,wherein the lateral condyle surface has a second plurality of radii of curvature between the first contact point and the second contact point on the lateral condyle surface to transition from the third radius of curvature to the fourth radius of curvature over a range of flexion,wherein the first degree of flexion is in the range of 0 degrees to 10 degrees, and the second degree of flexion is in the range of 45 degrees to 55 degrees,wherein a difference between the first radius of curvature and the second radius of curvature is different from a difference between the third radius of curvature and the fourth radius of curvature, andwherein the posterior cam of the femoral component initially contacts the spine of the tibial bearing at a fifth degree of flexion greater than the second degree of flexion and the fourth degree of flexion.
  • 16. The orthopaedic knee prosthesis of claim 15, wherein the fifth degree of flexion is greater than 60 degrees.
  • 17. The orthopaedic knee prosthesis of claim 15, wherein the fifth degree of flexion is in the range of 65 degrees to 75 degrees.
  • 18. The orthopaedic knee prosthesis of claim 15, wherein a first ratio of the first radius of curvature to the second radius of curvature is equal to a second ratio of the third radius of curvature to the fourth radius of curvature.
  • 19. The orthopaedic knee prosthesis of claim 15, wherein: the first radius of curvature of the medial condyle surface has an origin, the first plurality of radii of curvature of the medial condyle surface have a common origin, and a distance between the origin of the first radius of curvature and the common origin of the first plurality of radii of curvature is in the range of 0 and 10 millimeters, andthe third radius of curvature of the lateral condyle surface has an origin, the second plurality of radii of curvature of the lateral condyle surface have a common origin, and a distance between the origin of the third radius of curvature and the common origin of the second plurality of radii of curvature is in the range of 0 and 10 millimeters.
  • 20. The orthopaedic knee prosthesis of claim 15, wherein the medial condyle surface contacts the medial bearing surface at a third contact point on the medial condyle surface at a sixth degree of flexion greater than the second degree of flexion, the medial condyle surface in the sagittal plane has a fifth radius of curvature at the third contact point, and the fifth radius of curvature is greater than the second radius of curvature by at least 0.5 millimeters, and wherein the lateral condyle surface contacts the medial bearing surface at a third contact point on the lateral condyle surface at a seventh degree of flexion greater than the fourth degree of flexion, the lateral condyle surface in the sagittal plane has a sixth radius of curvature at the third contact point, and the sixth radius of curvature is greater than the fourth radius of curvature by at least 0.5 millimeters.
Parent Case Info

This application is a continuation of Utility patent application Ser. No. 16/391,512, now U.S. Pat. No. 10,849,760, which was filed on Apr. 23, 2019, which is a continuation of Utility patent application Ser. No. 15/949,546, now U.S. Pat. No. 10,265,180, which was filed on Apr. 10, 2018, which is a continuation of Utility patent application Ser. No. 15/145,573, now U.S. Pat. No. 9,937,049, which was filed on May 3, 2016, which is a continuation of Utility patent application Ser. No. 14/486,085, now U.S. Pat. No. 9,326,864, which was filed on Sep. 15, 2014, which is a continuation of Utility patent application Ser. No. 13/481,943, now U.S. Pat. No. 8,834,575, which was filed on May 28, 2012, which is a continuation of U.S. patent application Ser. No. 12/165,575, now U.S. Pat. No. 8,187,335, which was filed on Jun. 30, 2008, the entirety of each of which is hereby incorporated by reference.

US Referenced Citations (392)
Number Name Date Kind
3765033 Goldberg et al. Oct 1973 A
3840905 Deane Oct 1974 A
3852045 Wheeler et al. Dec 1974 A
3855638 Pilliar Dec 1974 A
3869731 Waugh et al. Mar 1975 A
4081866 Upshaw et al. Apr 1978 A
4156943 Collier Jun 1979 A
4206516 Pilliar Jun 1980 A
4209861 Walker et al. Jul 1980 A
4215439 Gold et al. Aug 1980 A
4249270 Bahler et al. Feb 1981 A
4257129 Volz Mar 1981 A
4262368 Lacey Apr 1981 A
4309778 Buechel et al. Jan 1982 A
4340978 Buechel et al. Jul 1982 A
4470158 Pappas et al. Sep 1984 A
4612160 Donlevy et al. Sep 1986 A
4673407 Martin Jun 1987 A
4714474 Brooks et al. Dec 1987 A
4795468 Hodorek et al. Jan 1989 A
4808185 Penenberg et al. Feb 1989 A
4822362 Walker et al. Apr 1989 A
4838891 Branemark et al. Jun 1989 A
4888021 Forte et al. Dec 1989 A
4938769 Shaw Jul 1990 A
4944757 Martinez et al. Jul 1990 A
4944760 Kenna Jul 1990 A
4950298 Gustilo et al. Aug 1990 A
4963152 Hofmann et al. Oct 1990 A
4990163 Ducheyne et al. Feb 1991 A
5007933 Sidebotham et al. Apr 1991 A
5011496 Forte et al. Apr 1991 A
5019103 Van Zile et al. May 1991 A
5037423 Kenna Aug 1991 A
5071438 Jones et al. Dec 1991 A
5080675 Ashby et al. Jan 1992 A
5104410 Chowdhary Apr 1992 A
5108442 Smith Apr 1992 A
5116375 Hofmann May 1992 A
5133758 Hollister Jul 1992 A
5147405 Van Zile et al. Sep 1992 A
5171283 Pappas et al. Dec 1992 A
5201766 Georgette Apr 1993 A
5219362 Tuke et al. Jun 1993 A
5236461 Forte Aug 1993 A
5251468 Lin et al. Oct 1993 A
5258044 Lee Nov 1993 A
5271737 Baldwin et al. Dec 1993 A
5282861 Kaplan Feb 1994 A
5308556 Bagley May 1994 A
5309639 Lee May 1994 A
5326361 Hollister Jul 1994 A
5330533 Walker Jul 1994 A
5330534 Herrington et al. Jul 1994 A
5344460 Turanyi et al. Sep 1994 A
5344461 Phlipot Sep 1994 A
5344494 Davidson et al. Sep 1994 A
5358527 Forte Oct 1994 A
5368881 Kelman et al. Nov 1994 A
5370699 Hood et al. Dec 1994 A
5387240 Pottenger et al. Feb 1995 A
5395401 Bahler Mar 1995 A
5405396 Heldreth et al. Apr 1995 A
5413604 Hodge May 1995 A
5414049 Sun et al. May 1995 A
5449745 Sun et al. Sep 1995 A
5458637 Hayes Oct 1995 A
5480446 Goodfellow et al. Jan 1996 A
5543471 Sun et al. Aug 1996 A
5549686 Johnson et al. Aug 1996 A
5571187 Devanathan Nov 1996 A
5571194 Gabriel Nov 1996 A
5609639 Walker Mar 1997 A
5609643 Colleran et al. Mar 1997 A
5639279 Burkinshaw et al. Jun 1997 A
5650485 Sun et al. Jul 1997 A
5658333 Kelman et al. Aug 1997 A
5658342 Draganich et al. Aug 1997 A
5658344 Hurlburt Aug 1997 A
5681354 Eckhoff Oct 1997 A
5683468 Pappas Nov 1997 A
5702458 Burstein et al. Dec 1997 A
5702463 Pothier et al. Dec 1997 A
5702464 Lackey et al. Dec 1997 A
5702466 Pappas et al. Dec 1997 A
5725584 Walker et al. Mar 1998 A
5728748 Sun et al. Mar 1998 A
5732469 Hamamoto et al. Mar 1998 A
5755800 O'Neil et al. May 1998 A
5755801 Walker et al. May 1998 A
5755803 Haines et al. May 1998 A
5765095 Flak et al. Jun 1998 A
5766257 Goodman et al. Jun 1998 A
5776201 Colleran et al. Jul 1998 A
5800552 Forte Sep 1998 A
5811543 Hao et al. Sep 1998 A
5824096 Pappas et al. Oct 1998 A
5824100 Kester et al. Oct 1998 A
5824102 Buscayret Oct 1998 A
5824103 Williams Oct 1998 A
5871543 Hofmann Feb 1999 A
5871545 Goodfellow et al. Feb 1999 A
5871546 Colleran et al. Feb 1999 A
5879394 Ashby et al. Mar 1999 A
5879400 Merrill et al. Mar 1999 A
5906644 Powell May 1999 A
5935173 Roger et al. Aug 1999 A
5951603 O'Neil et al. Sep 1999 A
5957979 Beckman et al. Sep 1999 A
5964808 Blaha et al. Oct 1999 A
5976147 Lasalle et al. Nov 1999 A
5984969 Matthews et al. Nov 1999 A
5989027 Wagner et al. Nov 1999 A
5997577 Herrington et al. Dec 1999 A
6004351 Tomita et al. Dec 1999 A
6005018 Cicierega et al. Dec 1999 A
6010534 O'Neil et al. Jan 2000 A
6013103 Kaufman et al. Jan 2000 A
6017975 Saum et al. Jan 2000 A
6039764 Pottenger et al. Mar 2000 A
6042780 Huang Mar 2000 A
6053945 O'Neil et al. Apr 2000 A
6059949 Gal-Or et al. May 2000 A
6068658 Insall et al. May 2000 A
6080195 Colleran et al. Jun 2000 A
6090144 Letot et al. Jul 2000 A
6123728 Brosnahan et al. Sep 2000 A
6123729 Insall et al. Sep 2000 A
6123896 Meeks et al. Sep 2000 A
6126692 Robie et al. Oct 2000 A
6135857 Shaw et al. Oct 2000 A
6139581 Engh et al. Oct 2000 A
6152960 Pappas Nov 2000 A
6162254 Timoteo Dec 2000 A
6174934 Sun et al. Jan 2001 B1
6206926 Pappas Mar 2001 B1
6210444 Webster et al. Apr 2001 B1
6210445 Zawadzki Apr 2001 B1
6217618 Hileman Apr 2001 B1
6228900 Shen et al. May 2001 B1
6238434 Pappas May 2001 B1
6242507 Saum et al. Jun 2001 B1
6245276 McNulty et al. Jun 2001 B1
6258127 Schmotzer Jul 2001 B1
6264697 Walker Jul 2001 B1
6280476 Metzger et al. Aug 2001 B1
6281264 Salovey et al. Aug 2001 B1
6299646 Chambat et al. Oct 2001 B1
6316158 Saum et al. Nov 2001 B1
6319283 Insall et al. Nov 2001 B1
6325828 Dennis et al. Dec 2001 B1
6344059 Krakovits et al. Feb 2002 B1
6361564 Marceaux et al. Mar 2002 B1
6372814 Sun et al. Apr 2002 B1
6379388 Ensign et al. Apr 2002 B1
6428577 Evans et al. Aug 2002 B1
6443991 Running Sep 2002 B1
6475241 Pappas Nov 2002 B2
6485519 Meyers et al. Nov 2002 B2
6491726 Pappas Dec 2002 B2
6494914 Brown et al. Dec 2002 B2
6503280 Repicci Jan 2003 B2
6506215 Letot et al. Jan 2003 B1
6506216 McCue et al. Jan 2003 B1
6524522 Vaidyanathan et al. Feb 2003 B2
6540787 Biegun et al. Apr 2003 B2
6558426 Masini May 2003 B1
6569202 Whiteside May 2003 B2
6582469 Tornier Jun 2003 B1
6582470 Lee et al. Jun 2003 B1
6589283 Metzger et al. Jul 2003 B1
6592787 Pickrell et al. Jul 2003 B2
6620198 Burstein et al. Sep 2003 B2
6623526 Lloyd Sep 2003 B1
6645251 Salehi et al. Nov 2003 B2
6660039 Evans et al. Dec 2003 B1
6660224 Lefebvre et al. Dec 2003 B2
6664308 Sun et al. Dec 2003 B2
6702821 Bonutti Mar 2004 B2
6719800 Meyers et al. Apr 2004 B2
6726724 Repicci Apr 2004 B2
6730128 Burstein May 2004 B2
6764516 Pappas Jul 2004 B2
6770078 Bonutti Aug 2004 B2
6770099 Andriacchi et al. Aug 2004 B2
6773461 Meyers et al. Aug 2004 B2
6797005 Pappas Sep 2004 B2
6818020 Sun et al. Nov 2004 B2
6846327 Khandkar et al. Jan 2005 B2
6846329 McMinn Jan 2005 B2
6849230 Feichtinger Feb 2005 B1
6852272 Artz et al. Feb 2005 B2
6869448 Tuke et al. Mar 2005 B2
6893388 Reising et al. May 2005 B2
6893467 Bercovy May 2005 B1
6916340 Metzger et al. Jul 2005 B2
6923832 Sharkey Aug 2005 B1
6926738 Wyss Aug 2005 B2
6942670 Heldreth et al. Sep 2005 B2
6972039 Metzger et al. Dec 2005 B2
6986791 Metzger Jan 2006 B1
7025788 Metzger et al. Apr 2006 B2
7048741 Swanson May 2006 B2
7066963 Naegerl Jun 2006 B2
7070622 Brown et al. Jul 2006 B1
7081137 Servidio Jul 2006 B1
7094259 Tarabichi Aug 2006 B2
7101401 Brack Sep 2006 B2
7104996 Bonutti Sep 2006 B2
7105027 Lipman et al. Sep 2006 B2
7147819 Bram et al. Dec 2006 B2
7160330 Axelson, Jr. et al. Jan 2007 B2
7175665 German et al. Feb 2007 B2
7255715 Metzger Aug 2007 B2
7261740 Tuttle et al. Aug 2007 B2
7297164 Johnson et al. Nov 2007 B2
7326252 Otto et al. Feb 2008 B2
7341602 Fell et al. Mar 2008 B2
7344460 Gait Mar 2008 B2
7357817 D'Alessio, II Apr 2008 B2
7422605 Burstein et al. Sep 2008 B2
7510557 Bonutti Mar 2009 B1
7527650 Johnson et al. May 2009 B2
7572292 Crabtree et al. Aug 2009 B2
7578850 Kuczynski et al. Aug 2009 B2
7608079 Blackwell et al. Oct 2009 B1
7611519 Lefevre et al. Nov 2009 B2
7615054 Bonutti Nov 2009 B1
7618462 Ek Nov 2009 B2
7628818 Hazebrouck et al. Dec 2009 B2
7635390 Bonutti Dec 2009 B1
7658767 Wyss Feb 2010 B2
7678151 Ek Mar 2010 B2
7678152 Suguro et al. Mar 2010 B2
7708740 Bonutti May 2010 B1
7708741 Bonutti May 2010 B1
7740662 Barnett et al. Jun 2010 B2
7749229 Bonutti Jul 2010 B1
7753960 Cipolletti et al. Jul 2010 B2
7771484 Campbell Aug 2010 B2
7776044 Pendleton et al. Aug 2010 B2
7806896 Bonutti Oct 2010 B1
7806897 Bonutti Oct 2010 B1
7837736 Bonutti Nov 2010 B2
7842093 Peters et al. Nov 2010 B2
7875081 Lipman et al. Jan 2011 B2
7922771 Otto et al. Apr 2011 B2
8187335 Wyss et al. May 2012 B2
8192498 Wagner et al. Jun 2012 B2
8206451 Wyss et al. Jun 2012 B2
8236061 Heldreth et al. Aug 2012 B2
8734522 Wyss et al. May 2014 B2
8784496 Wagner et al. Jul 2014 B2
8795380 Heldreth et al. Aug 2014 B2
8828086 Williams et al. Sep 2014 B2
8834575 Wyss et al. Sep 2014 B2
9452053 Wagner et al. Sep 2016 B2
9931216 Williams et al. Apr 2018 B2
9937049 Wyss et al. Apr 2018 B2
10179051 Heldreth et al. Jan 2019 B2
10265180 Wyss et al. Apr 2019 B2
10543098 Williams et al. Jan 2020 B2
10729551 Heldreth et al. Aug 2020 B2
10849760 Wyss et al. Dec 2020 B2
20020138150 Leclercq Sep 2002 A1
20030009232 Metzger et al. Jan 2003 A1
20030035747 Anderson et al. Feb 2003 A1
20030044301 Lefebvre et al. Mar 2003 A1
20030075013 Grohowski Apr 2003 A1
20030139817 Tuke et al. Jul 2003 A1
20030153981 Wang et al. Aug 2003 A1
20030171820 Wilshaw et al. Sep 2003 A1
20030199985 Masini Oct 2003 A1
20030212161 McKellop et al. Nov 2003 A1
20030225456 Ek Dec 2003 A1
20040015770 Kimoto Jan 2004 A1
20040039450 Griner et al. Feb 2004 A1
20040167633 Wen et al. Aug 2004 A1
20040186583 Keller Sep 2004 A1
20040215345 Perrone, Jr. et al. Oct 2004 A1
20040243244 Otto et al. Dec 2004 A1
20040243245 Plumet et al. Dec 2004 A1
20050021147 Tarabichi Jan 2005 A1
20050055102 Tornier et al. Mar 2005 A1
20050059750 Sun et al. Mar 2005 A1
20050069629 Becker et al. Mar 2005 A1
20050096747 Tuttle et al. May 2005 A1
20050100578 Schmid et al. May 2005 A1
20050123672 Justin et al. Jun 2005 A1
20050143832 Carson Jun 2005 A1
20050154472 Afriat Jul 2005 A1
20050203631 Daniels et al. Sep 2005 A1
20050209701 Suguro et al. Sep 2005 A1
20050209702 Todd et al. Sep 2005 A1
20050249625 Bram et al. Nov 2005 A1
20050278035 Wyss et al. Dec 2005 A1
20060002810 Grohowski Jan 2006 A1
20060015185 Chambat et al. Jan 2006 A1
20060036329 Webster et al. Feb 2006 A1
20060052875 Bernero et al. Mar 2006 A1
20060100714 Ensign May 2006 A1
20060178749 Pendleton et al. Aug 2006 A1
20060195195 Burstein et al. Aug 2006 A1
20060228247 Grohowski Oct 2006 A1
20060231402 Clasen et al. Oct 2006 A1
20060241781 Brown et al. Oct 2006 A1
20060257358 Wen et al. Nov 2006 A1
20060271191 Hermansson Nov 2006 A1
20060289388 Yang et al. Dec 2006 A1
20070061014 Naegerl Mar 2007 A1
20070073409 Cooney et al. Mar 2007 A1
20070078521 Overholser et al. Apr 2007 A1
20070100463 Aram et al. May 2007 A1
20070129809 Meridew et al. Jun 2007 A1
20070135926 Walker Jun 2007 A1
20070173948 Meridew et al. Jul 2007 A1
20070196230 Hamman et al. Aug 2007 A1
20070203582 Campbell Aug 2007 A1
20070219639 Otto et al. Sep 2007 A1
20070293647 McKellop et al. Dec 2007 A1
20080004708 Wyss Jan 2008 A1
20080021566 Peters et al. Jan 2008 A1
20080091272 Aram et al. Apr 2008 A1
20080097616 Meyers et al. Apr 2008 A1
20080114462 Guidera et al. May 2008 A1
20080114464 Barnett et al. May 2008 A1
20080119940 Otto et al. May 2008 A1
20080161927 Savage et al. Jul 2008 A1
20080195108 Bhatnagar et al. Aug 2008 A1
20080199720 Liu Aug 2008 A1
20080206297 Roeder et al. Aug 2008 A1
20080269596 Revie et al. Oct 2008 A1
20090043396 Komistek Feb 2009 A1
20090048680 Naegerl Feb 2009 A1
20090082873 Hazebrouck et al. Mar 2009 A1
20090084491 Uthgenannt et al. Apr 2009 A1
20090088859 Hazebrouck et al. Apr 2009 A1
20090125114 May et al. May 2009 A1
20090192610 Case et al. Jul 2009 A1
20090265012 Engh et al. Oct 2009 A1
20090265013 Mandell Oct 2009 A1
20090292365 Smith et al. Nov 2009 A1
20090295035 Evans Dec 2009 A1
20090306785 Farrar et al. Dec 2009 A1
20090319047 Walker Dec 2009 A1
20090326663 Dun Dec 2009 A1
20090326664 Wagner et al. Dec 2009 A1
20090326665 Wyss et al. Dec 2009 A1
20090326666 Wyss et al. Dec 2009 A1
20090326667 Williams et al. Dec 2009 A1
20090326674 Liu et al. Dec 2009 A1
20100016979 Wyss et al. Jan 2010 A1
20100036499 Pinskerova Feb 2010 A1
20100036500 Heldreth et al. Feb 2010 A1
20100042224 Otto et al. Feb 2010 A1
20100042225 Shur Feb 2010 A1
20100063594 Hazebrouck et al. Mar 2010 A1
20100070045 Ek Mar 2010 A1
20100076563 Otto et al. Mar 2010 A1
20100076564 Schilling et al. Mar 2010 A1
20100094429 Otto Apr 2010 A1
20100098574 Liu et al. Apr 2010 A1
20100100189 Metzger Apr 2010 A1
20100100190 May et al. Apr 2010 A1
20100100191 May et al. Apr 2010 A1
20100125337 Grecco et al. May 2010 A1
20100161067 Saleh et al. Jun 2010 A1
20100191341 Byrd Jul 2010 A1
20100222890 Barnett et al. Sep 2010 A1
20100286788 Komistek Nov 2010 A1
20100292804 Samuelson Nov 2010 A1
20100305710 Metzger et al. Dec 2010 A1
20100312350 Bonutti Dec 2010 A1
20110029090 Zannis et al. Feb 2011 A1
20110029092 Deruntz et al. Feb 2011 A1
20110035017 Deffenbaugh et al. Feb 2011 A1
20110035018 Deffenbaugh et al. Feb 2011 A1
20110106268 Deffenbaugh et al. May 2011 A1
20110118847 Lipman et al. May 2011 A1
20110125280 Otto et al. May 2011 A1
20110153026 Heggendorn et al. Jun 2011 A1
20120239158 Wagner et al. Sep 2012 A1
20120259417 Wyss et al. Oct 2012 A1
20120271428 Heldreth et al. Oct 2012 A1
20120296437 Wyss et al. Nov 2012 A1
20130006372 Wyss et al. Jan 2013 A1
20130006373 Wyss et al. Jan 2013 A1
20140228965 Wyss et al. Aug 2014 A1
20140303740 Heldreth et al. Oct 2014 A1
20140350686 Williams et al. Nov 2014 A1
20150005888 Wyss et al. Jan 2015 A1
20200163773 Williams et al. May 2020 A1
Foreign Referenced Citations (73)
Number Date Country
1803106 Jul 2006 CN
1872009 Dec 2006 CN
4308563 Sep 1994 DE
19529824 Feb 1997 DE
495340 Jul 1992 EP
510178 Oct 1992 EP
634155 Jan 1995 EP
634156 Jan 1995 EP
636352 Feb 1995 EP
732091 Sep 1996 EP
732092 Sep 1996 EP
765645 Apr 1997 EP
883388 Dec 1998 EP
1129676 Sep 2001 EP
1196118 Apr 2002 EP
1226799 Jul 2002 EP
1374805 Jan 2004 EP
1421918 May 2004 EP
1440675 Jul 2004 EP
1470801 Oct 2004 EP
1518521 Mar 2005 EP
1591082 Nov 2005 EP
1779812 May 2007 EP
1923079 May 2008 EP
2649965 Oct 2013 EP
2417971 Sep 1979 FR
2621243 Apr 1989 FR
2653992 May 1991 FR
2780636 Jan 2000 FR
2787012 Jun 2000 FR
2809302 Nov 2001 FR
2835178 Aug 2003 FR
1065354 Apr 1967 GB
2293109 Mar 1996 GB
2335145 Sep 1999 GB
56083343 Jul 1981 JP
62205201 Sep 1987 JP
H08500992 Feb 1996 JP
H08503407 Apr 1996 JP
08224263 Sep 1996 JP
2002291779 Oct 2002 JP
2004167255 Jun 2004 JP
2006015133 Jan 2006 JP
2010012261 Jan 2010 JP
7900739 Oct 1979 WO
8906947 Aug 1989 WO
9014806 Dec 1990 WO
9601725 Jan 1996 WO
9623458 Aug 1996 WO
9624311 Aug 1996 WO
9624312 Aug 1996 WO
9846171 Oct 1998 WO
9927872 Jun 1999 WO
9966864 Dec 1999 WO
0209624 Feb 2002 WO
03039609 May 2003 WO
03101647 Dec 2003 WO
2004058108 Jul 2004 WO
2004069104 Aug 2004 WO
2005009489 Feb 2005 WO
2005009729 Feb 2005 WO
2005072657 Aug 2005 WO
2005087125 Sep 2005 WO
2006014294 Feb 2006 WO
2006130350 Dec 2006 WO
2007106172 Sep 2007 WO
2007108804 Sep 2007 WO
2007119173 Oct 2007 WO
2008100784 Aug 2008 WO
2009046212 Apr 2009 WO
2009128943 Oct 2009 WO
2013003433 Jan 2013 WO
2013003435 Jan 2013 WO
Non-Patent Literature Citations (94)
Entry
Operative Technique the Turning Point, Accord, the Johnson/Elloy Concept, Chas FL Thackray Ltd, 32 pages. Publication date prior to Jun. 30, 2007.
Prosthesis and Instrumentation the Turning Point, Accord, the Johnson/Elloy Concept, Chas F. Thackray Ltd, 8 pages. Publication date prior to Jun. 30, 2007.
Ries, “Effect of ACL Sacrifice, Retention, or Substitution on K After TKA,” http://www.orthosupersite.com/view.asp?rID=23134, Aug. 2007, 5 pgs.
Signus Medizintechnik, “Peek-Optima.RTM., The Polymer for Implants, Technical Information for the Medical Professional”, 7 pages. Publication date prior to Jun. 30, 2007.
Scorpio Knee TS Single Axis Revision Knee System, Stryker Orthopaedics, http://www.stryker.com/stellent/groups/public/documents/web.sub.-prod/02-3609.pdf, (6 pages). Publication date prior to Jun. 30, 2007.
The Turning Point, Accord, the Johnson Elloy Concept, Chas F. Thackray Ltd, 20 pages. Publication date prior to Jun. 30, 2007.
Zimmer Nexgen Trabecular Metal Tibial Tray, The Best Thing Next to Bone, 97-5954-001-00, 2007, 4 pages.
European Search Report for European Patent Application No. 08253140.1-2310, dated Dec. 23, 2008, 7 pgs.
Koo, et al., “The Knee Joint Center of Rotation is Predominantly on the Lateral Side During Normal Walking”, Journal of Biomechanics, vol. 41 (2008): 1269-1273, 5 pages.
“NexGen Complete Knee Solution Cruciate Retaining Knee (CR),” Zimmer, available at: http://zimmer.com.au/ctl?template=PC&op=global&action=&template=PC&id=356—, downloaded on Feb. 18, 2009, (1 page).
Biomet, Vanguard Mono-Lock Tibial System, Patented Convertible Tibial Bearing Technology, 2009, 2 Pages.
European Patent Office, Search Report for App. No. 09164479.9-2310, dated Nov. 4, 2009, 6 pages.
European Seach Report for European Patent Application No. 09164235.5-1526, dated Dec. 22, 2009, 6 pgs.
European Search Report for European Patent Application No. 08164944.4-2310-2042131, dated Mar. 16, 2009, 12 pgs.
Japanese Search Report, Japanese Patent Application No. 2017-122056, dated Jun. 28, 2018, 6 pages.
European Search Report for European Patent Application No. 09164245.4-2310, dated Oct. 15, 2009, 5 pages.
European Search Report for European Patent Application No. 09164245A-2310, dated Oct. 15, 2009, 5 pgs.
European Search Report for European Patent Application No. 09164478.1-2310, dated Oct. 20, 2009, 6 Pages.
Indian Search Report, Indian Patent Application No. 929/KOL/2009, dated Jul. 16, 2018, 4 pages.
Japanese Search Report for Japanese Patent Application No. 2009-501393, dated Oct. 26, 2010, 5 Pages.
Japanese Search Report, Japanese Patent Application No. 2009-153350, dated Jun. 18, 2013, 4 pages.
Karachalios, et al., “A Mid-Term Clinical Outcome Study of the Advance Medial Pivot Knee Arthroplasty”, www.sciencedirect.come, The Knee 16 (2009); 484-488, 5 pages.
Mannan, et al., “The Medial Rotation Total Knee Replacement: A Clinical and Radiological Review at a Mean Follow-Up of Six Years”, The Journal of Bone and Joint Surgery, vol. 91-B, No. 6 (Jun. 2009): 750-756, 7 Pages.
Moonot, et al., “Correlation Between the Oxford Knee and American Knee Society Scores at Mid-Term Follow-Up”, The Journal of Knee Surgery, vol. 22, No. 3 (Jul. 2009), 226-230, 5 Pages.
Omori, et al., “The Effect of Geometry of the Tibial Polyethylene Insert on the Tibiofemoral Contact Kinematics in Advance Medical Pivot Total Knee Arthroplasty”, The Journal of Orthopaedics Science (2009), 14:754-760, 7 pages.
Vanguard Complete Knee System, Biomet, available at: http://www.biomet.com/patients/vanguard.sub.-complete.cfm, downloaded on Feb. 2009, (3 pages).
Zimmer, Trabecular Metal Monoblock Tibial Components, An Optimal Combination of Material and Design, www.zimmer.com, 2009, 3 pages.
Barnes, C.L., et al, “Kneeling is Safe for Patients Implanted With Medical-Pivot Total Knee Arthoplasty Designs, Journal of Arthoplasty”, vol. 00, No. 0 2010, 1-6, 6 pages. Dated 2010.
Depuy Orthopaedics, Inc., “Sigma Fixed Bearing Knees—Function with Wear Resistance”, 2010, 0612-65-508 (Rev. 1) 20 pages.
European Search Report for European Patent Application No. 06739287.8-2310, dated Mar. 16, 2010, 3 Pages.
European Search Report for European Patent Application No. 09164160.5-1526, dated Jan. 4, 2010, 4 pgs.
European Search Report for European Patent Application No. 09164168.8-1526, dated Jan. 4, 2010, 6 pgs.
European Search Report for European Patent Application No. 09164228.0-1526, dated Feb. 2, 2010, 6 pgs.
European Search Report for European Patent Application No. 09164478.1-2310, dated Apr. 28, 2010, 12 Pages.
European Search Report for European Patent Application No. 10162138.1, dated Aug. 30, 2010, 7 Pages.
European search report; European Application No. 10174439.9-1526; dated Dec. 20, 2010; 4 pages.
Extended European Search Report, European Application No. 10174439.9-1526, dated Dec. 20, 2010, 4 Pages.
Extended European Search Report, European Application No. 10174440.7-1526, dated Dec. 10, 2010, 4 Pages.
Fan,Cheng-Yu, et al., “Primitive Results After Medical-Pivot Knee Arthroplasties: A Minimum 5 Year Follow-Up Study”, The Journal of Arthroplasty, vol. 25, No. 3 2010, 492-496, 5 Pages.
European Search Report for European Patent Application No. 11150648.1-2310, dated Apr. 7, 2011, 4 pages.
European Search Report for European Patent Application No. 11150648.1-2310, dated Apr. 7, 2011, 5 pgs.
PCT Written Opinion of the International Searching Authority for Corresponding International App. Search Report PCT/US 12/44354, dated Sep. 24, 2012, 11 pages.
State Intellectual Property Office of People's Republic China; Chinese Search Report; Application No. 200910166935.6; dated Mar. 26, 2013; 2 pages.
Operative Technique, Johnson Elloy Knee System, Chas F. Thackray, Ltd., 1988, 34 pgs.
Shaw et al., “The Longitudinal Axis of the Knee and the Role of the Cruciate Ligaments in Controlling Transverse Rotation”, J.Bone Joint Surg. AM. 1974:56:1603-1609, 8 Pages.
Clary et al., “Kinematics of Posterior Stabilized and Cruciate Retaining Knee Implants During an in Vitro Deep Knee Bend,” 54th Annual Meeting of the Orthopaedic Research Society, Poster No. 1983, Mar. 2008.
Kurosawa, et al., “Geometry and Motion of the Knee for Implant and Orthotic Design”, The Journal of Biomechanics 18 (1985), pp. 487-499, 12 pages.
2nd Int'l Johnson-Elloy Knee Meeting, Mar. 1987, 9 pages.
Murphy, Michael Charles, “Geometry and the Kinematics of the Normal Human Knee”, Submitted to Masachusetts Institute of Technology (1990), 379 Pages.
Factors Affecting the Range of Movement of Total Knee Arthroplasty, Harvey et al, The Journal of Bone and Joint Surgery, vol. 75-B, No. 6, Nov. 1993, 6 pages.
Five to Eight Year Results of the Johnson/Elloy (Accord) Total Knee Arthroplasty, Johnson et al, The Journal of Arthroplasty, vol. 8, No. 1, Feb. 1993, 6 pages.
Depuy Inc., “AMK Total Knee System Product Brochure”, 1996, 8 pages.
Fuller, et al., “A Comparison of Lower-Extremity Skeletal Kinematics Measured Using Skin and Pin-Mounted Markers”, Human Movement Science 16 (1997) 219-242, 24 Pages.
Dennis et al., “In vivo anteroposterior femorotibial translation of total knee arthroplasty: a multicenter analysis,” Clin Orthop Rel Res, 356: 47-57, 1998.
Depuy Orthopaedics, Inc., “AMK Total Knee System Legent II Surgical Techinque”, 1998, 30 pages.
Procedure, References Guide for Use with P.F.C. Sigma Knee Systems, 1998, 8 pages.
Depuy PFC Sigma RP, “PFC Sigma Knee System with Rotating Platform Technical Monograph”, 1999, 0611-29-050 (Rev. 3), 70 pages.
Midvatus Approach in Total Knee Arthroplasty, a Description and a Cadaveric Study Determining the Distance of the Popliteal Artery From the Patellar Margin of the Incision, Cooper et al., The Journal of Arthoplasty, vol. 14 No. 4, 1999, 4 pages.
Advice Notice (NI) Mar. 2000, Defect & Investigation Centre, Mar. 13, 2000, 3 pages.
Goodfellow et al., “The Mechanics of the Knee and Prosthesis Design,” The Journal of Bone and Joint Surgery, vol. 60-B, No. 3, 12 pgs. Dated Mar. 16, 2000. Publication date prior to Jun. 30, 2007.
Hill, et al., “Tibiofemoral Movement 2: The Loaded and Unloaded Living Knee Studied by MRI” The Journal of Bone & Joint Surgery, vol. 82-B, No. 8 (Nov. 2000), 1196-1198, 3 Pages.
Nakagawa, et al., “Tibiofemoral Movement 3: Full Flexion of the Normal Human Knee”, J.Bone Joint Surg. AM, vol. 82-B, No. 8 (2000). 1199-1200, 2 Pages.
The Effects of Conformity and Load in Total Knee Replacement, Kuster, et al, Clinical Orthopaedics and Related Research No. 375, Jun. 2000.
Uvehammer et al., “In vivo kinematics of total knee arthroplasty: flat compared with concave tibial joint surface,” J Orthop Res 18(6): 856-64, 2000.
Asano et al. “In Vivo Three-Dimensional Knee Kinematics Using a Biplanar Image-Matching Technique,” Clin Orthop Rel Res, 388: 157-166, 2001, (10 pages).
D'Lima et al., “Quadriceps moment arm and quadriceps forces after total knee arthroplasty,” Clin Orthop Rel Res 393:213-20, 2001.
Bertin et al., “In Vivo Determination of Posterior Femoral Rollback for Subjects Having a NexGen Posterior Cruciate-Retaining Total Knee Arthroplasty,” J. Arthroplasty, vol. 17, No. 8, 2002, 9 pgs.
The Johnson Elloy (Accord) Total Knee Replacement, Norton et al, The Journal of Bone and Joint Surgery (BR), vol. 84, No. 6, Aug. 2002, 4 pages.
Walker, et al., “Motion of a Mobile Bearing Knee Allowing Translation of Rotation”, Journal of Arthroplasty 17 (2002): 11-19, 9 Pages.
Andriacchi, T.P., “The Effect of Knee Kinematics, Gait and Wear on the Short and Long-Term Outcomes of Primary Knee Replacement,” NIH Consensus Development Conference on Total Knee Replacement, pp. 61-62, Dec. 8-10, 2003, (4 pages).
Blaha, et al., “Kinematics of the Human Knee Using an Open Chain Cadaver Model”, Clinical Orthopaedics and Related Research, vol. 410 (2003); 25-34, 10 pages.
Dennis et al., “Multicenter Determination of In Vivo Kinematics After Total Knee Arthroplasty,” Clin. Orthop. Rel. Res., 416, 37-57, 21 pgs. Dated 2003.
Komistek, et al., “In Vivo Flouroscopic Analysis of the Normal Human Knee”, Clinical Orthopaedics 410 (2003): 69-81, 13 Pages.
Ranawat, “Design may be counterproductive for optimizing flexion after TKR,” Clin Orthop Rel Res 416: 174-6, 2003.
Dennis, et al. “A Multi-Center Analysis of Axial Femorotibial Rotation After Total Knee Arthoplasty” , Clinical Orthopaedics 428 (2004); 180-189, 10 Pages.
Komistek, et al., “In Vivo Polyethylene Bearing Mobility is Maintained in Posterior Stabilized Total Knee Arthroplasty”, Clinical Orthopaedics 428 (2004): 207-213, 7 pages.
Saari et al., “The effect of tibial insert design on rising from a chair; motion analysis after total knee replacement,” Clin Biomech 19(9): 951-6, 2004.
Carl Zeiss, Zeiss SURFCOMM 5000—“Contour and Surface Measuring Machines”, 2005, 16 pages.
Dennis et al., “In Vivo Determination of Normal and Anterior Cruciate Ligament-Deficient Knee Kinematics,” J. Biomechanics, 38, 241-253, 2005, 13 pgs.
Freeman, M.A.R., et al., “The Movement of the Normal Tibio-Femoral Joint”, The Journal of Biomechanics 38 (2005) (2), pp. 197-208, 12 Pgs.
P. Johal et al, “Tibio-femoral movement in the living knee. A study of weight bearing and non-weight bearing knee kinematics using ‘interventional’ MRI,” Journal of Biomechanics, vol. 38, Issue 2, Feb. 2005, pp. 269-276, (8 pages).
Wang et al., “A biomechanical comparison between the single-axis and multi-axis total knee arthroplasty systems for stand-to-sit movement,” Clin Biomech 20(4): 428-33, 2005.
Yoshiya et al., “In Vivo Kinematic Comparison of Posterior Cruciate-Retaining and Posterior Stabilized Total Knee Arthroplasties Under Passive and Weight-bearing Conditions,” J. Arthroplasty, vol. 20, No. 6, 2005, 7 pgs.
Li et al, “Anterior Cruciate Ligament Deficiency Alters the In Vivo Motion of the Tibiofemoral Cartilage Contact Points in Both Anteroposterior and Mediolateral Directions,” JBJS-Am, vol. 88, No. 8, Aug. 2006, 10 pgs.
PCT Notification Concerning Transmittal of International Prel. Report for Corresponding International App. No. PCT/US2006/010431, dated Jun. 5, 2007, 89 Pages.
PCT Notification concerning transmittal of International Preliminary Report for corresponding International Appl. No. PCT/US2006/010431, dated Dec. 2, 2008, 6 pages.
Shakespeare, et al., “Flexion After Total Knee Replacement. A Comparison Between the Medical Pivot Knee and a Posterior Stabilised Knee”, www.sciencedirect.com, The Knee 13 (2006): 371-372, 3 Pages.
Suggs et al., “Three-Dimensional Tibiofemoral Articular Contact Kinematics of a Cruciate-Retaining Total Knee Arthroplasty,” JBJS-Am, vol. 88, No. 2, 2006, 10 pgs.
Wang et al., “Biomechanical differences exhibited during sit-to-stand between total knee arthroplasty designs of varying radii,” J Arthroplasty 21(8): 1196-9, 2006.
Brent et al. Effects of Coronal Plane Conformity on Tibial Loading in TKA: A Comparison of AGC Flat Versus Conforming Articulations, Orthopaedic Surgery, Surgical Technology International, XVIII, 6 pages. Publication date prior to Jun. 30, 2007.
Depuy Knees International, “Sigma CR Porocoat.RTM.,” 1 page. Publication date prior to Jun. 30, 2007.
Elloy et al. The Accuracy of Intramedullary Alignment in Total Knee Replacement, Chas F. Thackray Ltd, 12 pages. Publication date prior to Jun. 30, 2007.
Johnson et al. Restoration of Soft Tissue Stability, Chas. F. Thackray, Ltd., 21 pages. Publication date prior to Jun. 30, 2007.
Kessler et al., “Sagittal curvature of total knee replacements predicts in vivo kinematics,” Clinical Biomechanics 22(1):52-58, 2007.
Related Publications (1)
Number Date Country
20210145595 A1 May 2021 US
Continuations (6)
Number Date Country
Parent 16391512 Apr 2019 US
Child 17108309 US
Parent 15949546 Apr 2018 US
Child 16391512 US
Parent 15145573 May 2016 US
Child 15949546 US
Parent 14486085 Sep 2014 US
Child 15145573 US
Parent 13481943 May 2012 US
Child 14486085 US
Parent 12165575 Jun 2008 US
Child 13481943 US