High performance femoral knee prostheses

Information

  • Patent Grant
  • 8394147
  • Patent Number
    8,394,147
  • Date Filed
    Tuesday, November 23, 2010
    14 years ago
  • Date Issued
    Tuesday, March 12, 2013
    11 years ago
Abstract
Knee prostheses featuring components that more faithfully replicate the structure and function of the human knee joint in order to provide, among other benefits: greater flexion of the knee in a more natural way by promoting or at least accommodating internal tibial rotation in a controlled way, replication of the natural screw home mechanism, and controlled articulation of the tibia and femur respective to each other in a more natural way. In a preferred embodiment, such prostheses include an insert component disposed between a femoral component and a tibial component, the insert component preferably featuring among other things a reversely contoured posterolateral bearing surface that helps impart internal rotation to the tibia as the knee flexes. Other surfaces can also be specially shaped to achieve similar results, preferably using iterative automated techniques that allow testing and iterative design taking into account a manageable set of major forces acting on the knee during normal functioning, together with information that is known about natural knee joint kinetics and kinematics.
Description
BACKGROUND

1. Field of the Invention


The invention relates generally to knee prostheses and, more specifically, to knee prostheses which more closely emulate the anatomy and function of the knee and thereby feature range of flexion, rotation of the tibia relative to the femur, the screw home mechanism, and other structural and functional characteristics of the actual knee joint.


2. General Background of the Invention


Disease and trauma affecting the articular surfaces of the knee joint are commonly treated by surgically replacing the ends of the femur and tibia with prosthetic femoral and tibial implants, and, in some cases, replacing the patella with a patella component. Such surgeries are sometimes referred to as total knee replacement (TKR). In TKR surgery, a surgeon typically affixes two prosthetic components to the patient's bone structure; a first to the patient's femur and a second to the patient's tibia. These components are typically known as the femoral component and the tibial component respectively.


The femoral component is placed on a patient's distal femur after appropriate resection of the femur. The femoral component is usually metallic, having a highly polished outer condylar articulating surface, which is commonly J-shaped.


A common type of tibial component uses a tray or plateau that generally conforms to the patient's resected proximal tibia. The tibial component also usually includes a stem that extends at an angle to the plateau in order to extend into a surgically formed opening in the patient's intramedullary canal. The tibial component and tibial stem are both usually metallic.


A plastic or polymeric (often ultra high molecular weight polyethylene) insert or bearing fits between the tray of the tibial component and the femoral component. This insert provides a surface against which the femoral component condylar portion articulates, i.e., moves in gross motion corresponding generally to the motion of the femur relative to the tibia.


Modern TKR's are tricompartmental designs; they replace three separate articulating surfaces within the knee joint: the patello-femoral compartment and the lateral and medial inferior tibio-femoral compartments. Most currently available TKR's are designed to articulate from a position of slight hyperextension to approximately 115 to 130° flexion. A tricompartmental design can meet the needs of most TKR patients even though the healthy human knee is capable of a range of motion (ROM) approaching 170°. However, there are some TKR patients who have a particular need to obtain high flexion in the knee joint. For many, a TKR that permits patients to achieve a ROM in excess of 130° is desirable to allow deep kneeling, squatting and sitting on the floor with the legs tucked underneath.


Additionally, a common complaint of TKR patients is that the replaced knee does not does function like a normal knee or “feel normal.” The replaced knee does not achieve normal knee kinematics or motion and generally has a more limited ROM than a normal knee. Currently available designs produce kinematics different than the normal knee during gait, due to the complex nature of the knee joint and the motion of the femur and tibia relative to one another during flexion and extension. For example, it is known that, in addition to rotating about a generally horizontal axis during flexion and extension, the tibia also rotates about its longitudinal axis. Such longitudinal rotation is typically referred to as either external or internal rotation, depending on whether reference is being made to the femur or tibia respectively.


Very few currently available designs allow this longitudinal rotation. One known method to allow rotation is a mobile-bearing knee prosthesis. In mobile-bearing knee prostheses, the insert has increased contact with the condyles of the femoral component and rotates on top of the tibial component. However, mobile-bearing knee prostheses are less forgiving of soft tissue imbalance, increasing the incidence of bearing spin-out and dislocation. Another concern is that the mobile-bearing prostheses create an additional interface and underside wear may occur.


Constructing a total knee prosthesis which replicates the kinematics of a natural knee has been an on-going challenge in the orthopaedic field. Several attempts have been made and are well known in the prior art, including those shown in U.S. Pat. Nos. 6,264,697 and 6,325,828. Conventional designs such as these, however, leave room for improvement in simulating the structure and operation of actual knee joints, in at least the aspects of range of motion, internal rotation of the tibia relative to the femur as the knee flexes, and rotation of the tibia relative to the femur in overextension in order to allow the knee to be stabilized more efficiently.


SUMMARY

Devices according to aspects of the invention achieve more faithful replication of the structure and function of the actual knee joint by, among other things, adoption and use of structure and shaping of at least the polymeric insert and the femoral component to cause these components to cooperate with each other in new and unconventional ways (at least in the art of prosthetics) at various stages throughout the range of knee motion.


According to certain aspects and embodiments of the invention, there is provided a knee prosthesis in which the insert features a lateral posterior surface which slopes in a distal direction (as compared to the corresponding medial posterior surface) as it continues toward the posterior aspect of the insert, in order to cooperate with the lateral condyle of the femoral component to impart internal rotation to the tibia as the knee flexes between substantially 0 and substantially 130 degrees of flexion, to allow the prosthesis to induce or allow tibial internal rotation in a controllable manner as a function of flexion, to reduce the forces of any femoral component cam acting upon a post or other raised portion of the insert, or any combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis in which the insert features a greater thickness in certain lateral portions to increase durability, accommodate a more anatomic femoral component which features a lateral condyle smaller in some dimensions than its medial condyle, to impart a joint line more accurately replicating natural physiology, or any combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis in which the insert features more anatomic sulcus placement in order improve operation of the prosthesis by more anatomically applying forces imposed on the prosthesis by quadriceps and the patellar tendon, allow the prosthesis to replicate natural anatomy more effectively, or any combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis in which the insert features a lateral surface that is curved or “swept” in plan, in order to allow the lateral condyle to track in arcuate fashion on the bearing surface at certain ranges of knee flexion and rotation, to assist in facilitating the screw home mechanism, or combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis in which the insert features a post or other raised portion whose anterior surface is shaped to serve effectively as an anterior cruciate ligament when engaged with a cam during ranges of flexion such as after heel strike upon actuation of the quadriceps.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis in which the insert features a post or other raised portion whose posterior surface is shaped to assist internal rotation of the tibia relative to the femur as the knee flexes, such as starting at angles such as in a range of substantially 50 or more degrees, to help ensure that post/cam forces are directed net anteriorly, or a combination of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis in which the insert features rounded or chamfered peripheral edges to help reduce wear on surrounding tissue and/or for other purposes.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis with any desired combination or permutation of any of the foregoing features, properties or results.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component that includes a lateral condyle that is in some distal and posterior aspects smaller than corresponding dimensions of the medial condyle, in order to simulate more closely natural physiology, allow adequate insert thickness under the lateral condyle so that, for instance, the posteriolateral surface of the insert can feature convexity or slope, assist internal rotation of the tibia relative to the femur as the knee flexes from substantially 0 degrees to substantially 130 degrees, or any combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component that includes a lateral condyle with anterior surfaces more pronounced than corresponding anterior surfaces on the medial condyle, in order to replicate more closely natural anatomic structures in retaining the patella in lower ranges of flexion, cause the patella or substitute structure to track more physiologically at such ranges of motion, cause the quadriceps more physiologically to apply force to the prosthetic components and tibia in lower ranges of flexion, or any combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component that includes a cam that cooperates with a post or other raised portion on the insert to assist internal rotation on the tibia, ensure that cam/post forces are directed net anteriorly or a combination of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component that includes an anterior cam which cooperates with a post or other raised portion on the insert to simulate action of the anterior cruciate ligament at lower ranges of flexion.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component and an insert in which during operation in situ, the femoral component is situated more anteriorly on the insert at low angles of flexion than in conventional knee prostheses, in order to reduce the forces on the post of the insert, to resemble more closely actual operation and kinematics of the knee, or a combination of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component and an insert which during operation in situ reduces paradoxical motion and actual cam to post contact, and when there is contact, reduces impact of contact and force of contact, between the femoral component cam and the insert post or other raised portion during desired ranges of motion.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis including a femoral component which features a backdrafted anterior slope of the interior surfaces of the posterior condylar portions, in order to allow the distal portion of the femur to be resected so that the anterior cut and the posterior cut are not parallel, such that the distal extremity of the femur is physically greater in anterior-posterior dimension than portions more proximal, whereby the distal extremity of the femur can be physically captured by the interior surfaces of the femoral component.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis which helps impart internal rotation to the tibia as the knee flexes from substantially 0 degrees of flexion to substantially 130 degrees of flexion, such that the tibia is substantially fully internally rotated to an angle of at least approximately 8 degrees in order to allow such flexion to occur in more physiological fashion, to reduce the possibility that the quadriceps will pull the patella undesirably relative to the knee in a lateral direction (lateral subluxation), to allow the patella or its replacement to track the trochlear groove, or any combinations of these.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis which helps impart internal rotation of the tibia as the knee flexes between substantially zero degrees and substantially 130 degrees, to at least substantially 8 degrees of internal rotation of the tibia relative to the femur at flexion angles greater than 130 degrees.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis which imparts internal rotation of the tibia relative to the femur as the knee flexes from substantially 0 degrees to substantially 130 degrees of flexion, so that the tibia is substantially fully internally rotated relative to the femur to an angle of at least substantially 8 degrees at a flexion angle of substantially 130 degrees, such flexion and internal rotation of the tibia being facilitated at least in part by a twisting moment created by contact of the condyles of the femoral component on the insert.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis which imparts internal rotation of the tibia relative to the femur as the knee flexes from substantially 0 degrees to substantially 130 degrees of flexion, so that the tibia is substantially fully internally rotated relative to the femur to an angle of at least substantially 8 degrees at a flexion angle of substantially 130 degrees, such flexion and internal rotation of the tibia being facilitated at least in part by a twisting moment created by contact between the post or other raised portion of the insert and at least one cam of the femoral component.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis whose structure facilitates the screw home mechanism.


According to certain aspects and embodiments of the invention, there is further provided a knee prosthesis which allows flexion at flexion angles greater than 130 degrees while allowing internal rotation of the tibia relative to the femur as the knee flexes from substantially 0 degrees to substantially 130 degrees, without the need for a mobile bearing design or to allow the insert to swivel or rotate relative to the tibial component.


According to certain aspects and embodiments of the invention, there are provided methods of designing knee prosthetic components using simulation of a femoral, patella and insert structure, physiological data regarding structure and function of natural knees, and applying at least six force vectors to the structure throughout a desired range of motion to effectively and efficiently simulate forces applied to the tibia in the body: force applied by the patella ligament, ground reaction force, relative force applied by the lateral condyle on the insert, relative force applied by the medial condyle on the insert, force applied by the hamstring muscles, and relative force applied by the cam surfaces of the femoral component on the post or other raised portion of the insert.


According to certain aspects and embodiments of the invention, there are provided methods of designing knee prosthetic components using simulation of a femoral and insert structure and applying to the structure throughout a desired range of motion, force vectors that represent relatively greater forces applied by some ligaments, tendons and muscles than others, such as the relatively great forces applied by the quadriceps when they actuate and by the hamstrings when they actuate.


According to certain aspects and embodiments of the invention, there are provided methods of designing knee prosthetic components using simulation of a femoral and insert structure and applying to the structure a desired set of forces, evaluating the performance of the structure, modifying the structure as simulated in the computer, and repeating the process until a desired design is reached.


According to additional aspects and embodiments of the invention, there is provided a knee prosthesis comprising: a femoral component adapted to fit on a distal end of a femur, the femoral component including a lateral condylar structure and a medial condylar structure, the geometry of the lateral condylar structure being different from the geometry of the medial condylar structure; and an accommodation structure including a lateral proximal surface adapted to cooperate with the lateral condylar structure of the femoral component, and a medial proximal surface adapted to cooperate with the medial condylar structure of the femoral component, the geometry of the lateral proximal surface and the medial proximal surface being different from each other, to assist in imparting internal rotation on the tibia relative to the femoral component as the knee flexes from substantially zero degrees of flexion to substantially 130 degrees of flexion.


According to additional aspects and embodiments of the invention, there is provided a knee prosthesis comprising a femoral component adapted to fit on a distal end of a femur, the femoral component including: an anterior portion which includes an interior surface adapted to interface with the femur; a lateral condylar structure which includes a posterior section which in turn includes an interior surface adapted to interface with the femur; and a medial condylar structure which includes a posterior section which in turn includes an interior surface adapted to interface with the femur; wherein the interior surfaces are adapted to physically capture at least a portion of the femur in the femoral component relative to a distal translation substantially parallel to the anatomic axis of the femur; and wherein all interior surfaces of the femoral component are adapted to allow the femoral component to clear resected portions of the femur physically as the femoral component is rotated onto the femur about its posterior portions during installation.


Certain embodiments and aspects of the invention also provide other characteristics and benefits, and other objects, features and advantages of various embodiments and aspects of the invention will be apparent in the other parts of this document.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1A shows a perspective view of a left knee prosthesis according to an embodiment of the invention.



FIGS. 1B-1C show an exploded front perspective view of a femoral component and an insert of a left knee prosthesis according to an embodiment of the invention.



FIG. 2 shows an exploded back perspective view of a femoral component and an insert of a left knee prosthesis according to an embodiment of the invention.



FIG. 3 shows an exploded front perspective view of a femoral component and an insert of a left knee prosthesis according to an embodiment of the invention.



FIG. 4 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the left knee at full extension.



FIG. 5 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 30° flexion.



FIG. 6 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 60° flexion.



FIG. 7 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 90° flexion.



FIG. 8 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 120° flexion.



FIG. 9 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 130° flexion.



FIG. 10 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 140° flexion.



FIG. 11 is a side view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 150° flexion.



FIG. 12 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at full extension.



FIG. 13 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 30° flexion.



FIG. 14 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 60° flexion.



FIG. 15 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 90° flexion.



FIG. 16 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 120° flexion.



FIG. 17 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 130° flexion.



FIG. 18 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 140° flexion.



FIG. 19 is a top plan view of portions of a left knee prosthesis according to an embodiment of the invention showing the kinematics of the knee at 150° flexion.



FIG. 20 shows a front plan view of a left knee prosthesis according to an embodiment of the invention.



FIG. 21 shows certain aspects of a femoral component of a knee prosthesis according to an embodiment of the invention.



FIG. 22 shows certain aspects of a cam of a femoral component of a knee prosthesis according to an embodiment of the invention.



FIG. 23 shows certain aspects of a proximal surface of an insert of a knee prosthesis according to an embodiment of the invention.



FIG. 24 is a cross sectional view showing certain aspects of a lateral bearing surface of a knee prosthesis according to an embodiment of the invention.





DETAILED DESCRIPTION

Various embodiments of the invention provide improved knee prostheses for replacing at least a portion of a knee joint between the distal end of a femur and the proximal end of a tibia.


While not wishing to be bound by any particular theory, the inventors have discovered that knee prostheses which more faithfully and closely replicated the function, anatomy and physiology of the normal human knee would yield a number of advantages. Among other things, such prostheses would provide an increased range of motion and would function more normally particularly in extension, deep flexion and during normal gait. They would take into account the forces imposed on the knee by quadriceps and hamstrings actuation, forces which great in magnitude but not fully considered in conventional knee prosthesis design. Knee prostheses according to various aspects of the invention recognize that during movement of the knee, particularly during flexion, the position and orientation (kinematics) of the bones of the knee are a result of achieving equilibrium of the forces that cause motion of the knee (kinetics). Additionally, the shape of the articular surfaces (anatomy) acting in combination with forces imposed by various muscles, ligaments and tendons, determines the direction of the large contact forces. Therefore, aspects of the invention take into account that anatomy influences kinetics and kinetics determine kinematics.


Conventional knee prostheses have been developed without recognition of the full range of kinetics of active knee movement. Many are primarily concerned with achieving greater flexion. However, in addition to flexion and extension, motion of the knee is both rotational and translational. The femoral condyles both roll and glide as they articulate with respect to the tibial plateaus. As the knee moves from full extension into flexion the axis of rotation between the femur and the tibia moves posteriorly relative to both the femur and the tibia. Additionally, in the normal human knee, internal rotation of the tibia relative to the femur occurs as the knee flexes between full extension and approximately 130° of flexion. Knee prostheses according to various aspects of the invention provide various surfaces on at least the femoral component and the insert which promote such greater flexion, the screw home mechanism, internal rotation of the tibia relative to the femur as the knee flexes, and other characteristics of the natural knee.


According to some aspects of the invention, the design of knee prosthesis components is conducted using a process which (1) tests various performance aspects of a proposed design using computer simulation of the design and various forces imposed upon it, (2) allows analysis of the test results for development of improvements to the proposed design; (3) uses test results to change the proposed design (either manually or automatically), (4) tests various performance aspects of the modified design using computer simulation of the design and various forces imposed upon it, and (5) repeats these tasks in an iterative fashion until the performance testing shows an iteratively modified design to feature acceptable performance characteristics. It is also significant that in such performance testing, the performance of the proposed design is tested using forces that occur at various points in various activities, so that the performance testing is dynamic across extended ranges of motion and takes into account considerable forces placed on the design by actuation of the quadriceps and hamstring muscles, for example, and the consequent kinetic and kinematic effects of such forces.


A preferred embodiment of a knee prosthesis according to the invention is shown in FIGS. 1A-1C and 2-4, and identified by the numeral 100. The knee prosthesis 100 shown in these figures is designed to replace at least a portion of a left knee joint between the distal end of a femur and the proximal end of a tibia. A mirror image (not shown) of knee prosthesis 100 will replace at least a portion of a right knee between the distal end of a femur and the proximal end of a tibia.


The knee prosthesis 100 includes a femoral component 200 for mounting to a distal end of a femur, a tibial component 300 for mounting to a proximal end of a tibia, and an insert 400.


Embodiments of the femoral component 200 preferably include a medial condylar section 202, a lateral condylar section 204 and a trochlear groove 206 joining the anterior portions 214, 216 of the medial and lateral condylar sections 202, 204 together. The medial and lateral condylar sections 202, 204 are disposed apart from one another to form an intercondylar recess or notch 208. Each condylar section 202, 204 has an outer surface 210, 212 for engaging a tibial component 300 or insert 400 as will become apparent. The outer surfaces 210, 212 of each condylar section 202, 204 preferably have distal portion 218, 220 for engaging a portion of the tibial component 300 or insert 400 when the knee joint is extended and partially flexed, and posterior portions 222, 224 for engaging a portion of the tibial component 300 or insert 400 when the knee joint is flexed at angles of substantially 90° or greater.


Embodiments of a femoral component 200 according certain aspects of this particular nonlimiting embodiment of the invention also replicate the physiological joint line 227 of a normal knee as shown in FIG. 20. The physiological joint line 227 may be considered to be a line extending between the distal most portions of each condyle at a knee flexion angle of zero degrees. This physiological joint line is oriented at an angle of approximately 93 degrees from the mechanical axis of the leg (which could also be considered to be 87 degrees from the mechanical axis of the leg depending on perspective), or approximately 3 degrees from horizontal as shown in FIG. 20. The joint line established by prostheses according to certain embodiments and aspects of the invention preferably replicate this physiological joint line 227 as shown in that drawing.


Embodiments of the femoral component 200 preferably have a thickness approximately matching the bone resection necessary for the total knee replacement.


Embodiments of the femoral component 200 also preferably have a lateral condylar section 204 that is different in geometry than the geometry of the medial condylar section 202. In the embodiment shown in FIG. 1, the size of lateral condylar section 204 is smaller than the size of medial condylar section 202 so that its outer surface distal portion 220 does not extend as far distally as does the outer surface distal portion 218 of medial condylar section 202.


The femoral component 200 may include a rounded medial profile. According to certain embodiments, for example, it may feature a medial profile which includes a single radius from 15-160°, and may also include a lateral profile that is less round or curved distally, with a single radius from 10-160°.


In the normal human knee, the patella glides caudally on the femoral condyles from full extension to full flexion. By 20 to 30° of flexion, the patella first begins to articulate with the trochlear groove. At extreme flexion, the patella lies in the intercondylar recess. Initially the patella contact occurs distally and with increased flexion the contact areas shift proximally on the patella. Patellofemoral contact force is substantially body weight when walking, and increases to substantially 5 times body weight when stair climbing. These contact forces therefore impose a substantial load on the knee joint, which prostheses according to certain embodiments and aspects specifically take into account.


Knee prostheses according to certain embodiments and aspects of the invention incorporate features that allow the patellar implant of the knee prostheses to move in a way similar to the normal human knee and to withstand the normal patellofemoral contact force without unnecessary ligament release. These features include various aspects of the shape of portions of the medial condylar section 202 and the lateral condylar section 204, to be more consistent with natural anatomical geometry. For instance, anterior portion 216 of lateral condylar section 204 can be configured to extend further anteriorly than anterior portion 214 of medial condylar section 202, or to be more abruptly shaped on its surface that cooperates with the patella, so that it acts as a buttress to guide the patella at low flexion angles and in extension.


Femoral components according to certain embodiments and aspects of the invention can also include a patella-friendly trochlear groove 206. The trochlear groove 206 in such embodiments is substantially S-shaped and lateralizes the patella 500. The trochlear groove 206 further allows for a smooth transition between the anterior portions 214, 216 of the condylar sections and intercondylar notch 208. This further reduces the contact forces on the patella 500.


Femoral components 200 according to certain embodiments and aspects of the invention can include flexed or backdrafted substantially planar interior or bone interface surfaces 223 and 225 (collectively, backdrafted surface 229), on the anterior surfaces of posterior portions of medial condyle section 222 and lateral condyle section 224. Preferably, the interior surfaces 223, 225 are coplanar and are oriented so that their planes converge with a plane formed by the interior surface 215 on the posterior side of anterior portions 214 and 216 of the femoral component 200 as shown more clearly in FIG. 21. In this way, proximal portions of these posterior condylar interior surfaces 223 and 225 are located closer to the plane of the interior surface 215 of the anterior portion of the femoral component 200 than are distal portions of surfaces 223 and 225. Preferably, the convergence angle is in a range of between 1 and 30 degrees, and more preferably, the convergence angle is approximately 15 degrees. The backdrafted surface 229 extends the articular surface of the femoral component 200 with minimal bone resection. Removing less bone decreases the likelihood of later femoral fracture. It also minimizes the likelihood that the femoral component 200 will be forced off the end of the femur in deep flexion, since it serves to lock onto or capture the distal end of the femur in the femoral component 200.


The femoral component 200 with the backdrafted surface 229 can be installed by hinging and rotating the femoral component 200 onto the resected femur about the posterior portions of the condyles of the femur. The inventors have discovered that it is possible, by configuring all anterior surfaces of the femoral component 200 correctly, as shown in FIGS. 4-11 and 21, for example, to allow those surfaces to physically clear the resected bone as the femoral component is rotated onto the femur during installation. Among other ways to accomplish this configuration are: (1) to cause the interior surfaces to create a shallow interior space; and/or (2) to adjust angles and/or dimensions of the chamfered surfaces that connect the interior surfaces 223, 225 of condylar sections 202 and 204 and/or interior surface 215 of the anterior portion of the component 200 to the bottom interior surface of the component 200.


Interior surfaces of the component 200, including surfaces 215, 223 and 225, need not be planar or substantially planar to accomplish the objective of capturing or locking onto the femur. For instance, one or more of them may be curved or partially curved and accomplish this objective by orienting one or both of the interior surfaces of the condylar sections 202, 204 relative to the interior surface of the anterior portion of the femoral component at other than parallel.


Certain embodiments of the femoral component 200 may include an anterior cam 230, as shown in FIGS. 4-11. As explained further below, the anterior cam 230 works with the post or other raised portion 422 of the insert 400 to provide anterior stabilization during early gait. The anterior cam 230 preferably includes a large radius to increase the contact area between the anterior cam 230 and the post 422. The anterior cam surface 230 preferably does not engage the anterior surface of the post 422 for approximately 1-2 mm.


Certain embodiments of the femoral component 200 may include a posterior cam 232 as shown in FIGS. 4-11, among other places as well as in a closer view in FIG. 22. Preferably, the posterior cam 232 is asymmetrical. The lateral side 238 may be larger than the medial side 240, for example, as shown in FIG. 22. As explained further below, the larger lateral side 238 provides optimal contact between the posterior cam 232 and the post 422 during axial rotation, to assist in imparting internal rotation to the tibia relative to the femur as the knee flexes. In general, the posterior cam 232 engages the post 422 between 50-60° flexion. The post 422 may be thickened distally for additional strength.


Prostheses according to certain embodiments of the invention, which do not need to serve a posterior stabilization function, such as those which can be characterized as cruciate retaining, need not have a post or other raised surface 422 on insert 400, or cams, such as cams 232 or 230. In such embodiments and aspects, other surfaces such as portions of the medial and lateral condylar sections 202, 204 acting without a post or raised surface 422, for example, achieve or help achieve objectives of aspects of the invention, including allowing or imparting internal rotation to the tibia relative to the femur as the knee flexes, such as from substantially 0 degrees to substantially 130 degrees.


Certain embodiments of the femoral component 200 may include conventional attachment aids for helping to secure the femoral component 200 to a distal end of a femur. Such attachment aids may include one or more pegs, fins, surface treatments including bone ingrowth surfaces, surfaces for accommodating spacers, shims or other structures, or as otherwise desired.


Tibial components 300 according to certain embodiments and aspects of the invention include a tray or base member for being secured to a proximal end of a tibia. The base member can include a stabilizing post, which is insertable into the tibial medullary canal and provides for the stabilization of the tibial component 300 on the tibia.


Tibial components according to embodiments and aspects of the invention feature a tray member which includes a proximal or upper surface, a distal or lower surface, a medial surface, a lateral surface, an anterior or front surface, and a posterior or rear surface. The proximal surface may be substantially flat and planar. The tray member preferably includes attachment aids for helping to secure the tray member to a proximal end of a tibia. Such attachment aids may include one or more pegs, fins, screws, surface treatments, etc.


Femoral components 200 and tibial components 300 according to certain embodiments and aspects of the invention may be constructed in various manners and out of various materials. For example, the femoral component 200 and tibial component 300 may be machined, cast, forged or otherwise constructed as a one-piece integral unit out of a medical grade, physiologically acceptable metal such as a cobalt chromium alloy or the like, in various sizes to fit a range of typical patients, or may be custom-designed for a specific patient based on data provided by a surgeon after physical and radiography examination of the specific patient.


Inserts 400 according to certain embodiments and aspects of the invention include a proximal or upper surface 402, a distal or lower surface 404, a medial surface 406, a lateral surface 408, an anterior or front surface 410, and a posterior or rear surface 412. For convenience, such an insert 400 may be considered to feature a medial side 414 and a lateral side 416, corresponding to medial and lateral sides of the limb in which the insert is to be installed.


The proximal surface 402 of the particular insert 400 according to one embodiment of the invention shown in the drawings has a medial portion 418 for engaging the outer surface 210 of the medial condylar section 202 of the femoral component 200, and a lateral portion 420 for engaging the outer surface 212 of the lateral condylar section 204 of the femoral component 200.


Inserts 400 according to certain embodiments and aspects of the invention can include a central post or raised portion 422 as shown in the drawings. The post 422 includes a proximal surface 424, an anterior surface 426, a posterior surface 428 and medial and lateral side surfaces 430, 432. The anterior surface 426 of post 422 in an embodiment of the insert, is tapered or curved at a desired angle with respect to the distal surface 404 of the insert 400 to minimize impingement of the patella or a patellar implant 500 in deep flexion. The base can be tapered as desired in a posterior direction from the anterior surface 426 to minimize impingement of the intercondylar notch 208 of femoral component 200 in hyperextension.


Inserts 400 of certain embodiments and aspects of the invention as shown in the drawings include an anterior curved surface. The anterior curved surface allows room for the patellar tendon (not shown). The insert may also include a posterior curved surface. The result of the posterior curved surface is the removal of material that may impinge on the posterior cortex of the femur in deep flexion. The radius of curvature may vary as desired to provide sufficient room for maximal flexion.


The distal surface of the insert 400 according to certain embodiments and aspects of the invention may be substantially flat or planar for contacting the proximal surface of the tray member of the tibial component 300. The distal surface preferably includes a dovetail or other appropriate locking mechanism that consists of an anterior portion and a posterior portion. However, any conventional method for positioning and/or retaining the insert relative to the tray member, whether constrained or unconstrained, may be used. In other embodiments, the insert 400 may be allowed to articulate relative to the tray of the tibial component 300.


On the proximal surface 402 of inserts 400 according to certain embodiments and aspects of the invention, parts of the medial portion 418 of the proximal surface and parts of the lateral portion 420 are shaped to cooperate with outer surfaces 210 of the medial condylar section of femoral component 200 and outer surfaces 212 of the lateral condylar section of the femoral component, as the knee flexes and extends. These parts are referred to as medial insert bearing surface 440 and lateral insert bearing surface 442.


From a sagittal aspect, as shown in FIGS. 4-11 and also in FIGS. 23 and 24, posterior parts of the lateral bearing surface 442 of the particular insert shown in the drawings features a reverse slope; that is, the lateral bearing surface slopes toward the bottom or distal surface of the insert 400 as the lateral bearing surface progresses toward the posterior or back periphery of the insert 400, preferably either through a convex arc or a straight slope. The purpose of the slope is to change the direction of the contact force between the lateral bearing surface 442 and the lateral condylar section 204, in order to add an anterior force on the lateral bearing surface 442 greater than a corresponding anterior force on the medial bearing surface 440 at some angles of knee flexion, to produce or help produce a twisting moment about the longitudinal axis of the tibia or impart or assist in imparting internal rotation of the tibia as the knee flexes. Preferably, this rotation-imparting surface 444 is configured to impart or assist inward tibial rotation relative to the femur as the knee flexes between substantially 0 degrees of flexion to substantially 130 degrees of flexion, the internal rotation angle achieving a magnitude of at least substantially 8 degrees at substantially 130 degrees of knee flexion. Since the contact force vector is perpendicular to the lateral bearing surface 442, during rollback in the lateral compartment, a component of the contact force vector is generally parallel to the generally anteriorly oriented contact vector acting on the post 422. Accordingly, this contact force not only can help delay engagement of the post 422 with the posterior cam 232, but it can also beneficially reduce the force required by the post 422 to produce lateral rollback, resist anterior motion of the femoral component 200 relative to the insert 400, and resist total force which is absorbed by the post 422 in accomplishing posterior stabilization of the knee.


It is also possible to generate the tibial inward rotation inducing couple on the insert 400 by the femoral component 200 not only by using the posterior cam 232 as discussed below, but also by altering the shape of parts of the medial insert bearing surface 440 or using other structures, surface shaping or other techniques, or any combination of them, as desired.


Preferably, the lateral insert bearing surface 442 of the insert as shown in the drawings features a curved generally concave portion which sweeps laterally from its anterior extremity to approximately its middle, and then back medially from its middle to its posterior extremity, as shown in FIG. 23, for example. Such a swept surface helps guide the lateral condylar section 202 as the locus of its contact points with the insert 400 move in a posterior direction as the knee flexes.


Inserts 400 according to certain embodiments and aspects of the invention may be constructed in various manners and from various materials. For example, they may be machined, molded or otherwise constructed as a one-piece, integral unit out of medical grade, physiologically acceptable plastic such as ultra high molecular weight polyethylene or the like, in various sizes to fit a range of typical patients, or may be custom-designed for a specific patient based on data provided by a surgeon after physical and radiographic examination of the specific patient. The material can be treated, for example, by radiation, chemistry, or other technology to alter its wear properties and/or strength or hardness. Portions of various surfaces of inserts 400 can be treated with radiation, chemicals or other substances or techniques to enhance wear resistance properties; they can also be subjected to suitable surface treatments for such purposes and others.


If the medial condylar section 202 and the lateral condylar section 204 of the femoral component 200 were the same size, the insert 400 shown in the drawings would be thinner between its lateral insert bearing surface 442 and its distal surface 404 than between its medial insert bearing surface 440 and that distal surface 404. Such thinness may become unacceptable in regions between the rotation inducing surface 444 and the distal surface 404 in the posteriolateral region of the insert 400. To compensate, lateral parts of the insert 400 may be created thicker than medial parts, as shown for example in FIG. 20, so that the lateral insert bearing surface 442 is “higher” or more proximal than the medial insert bearing surface 440. In certain embodiments of the insert 400 as shown for example in FIG. 20, a line drawn between the most distal part of the medial insert bearing surface 440 and the most distal part of the lateral insert bearing surface 442 and denominated physiological joint line 227, forms an approximately 3 degree angle from a line perpendicular to the mechanical axis of the leg or in many insert 400 structures, substantially 3 degrees from the plane of the distal surface of the insert 400. This 3 degree angle is similar to the structure of the human knee, where the physiological joint line is usually substantially 3 degrees from the mechanical axis of the joint. The lateral contact point 436 of the femoral component 200 and the insert 400 is initially higher than the medial contact point 434. During flexion, as the lateral condyle 204 rolls posteriorly, the lateral femoral condyle 204 moves down the arc or slope of tibial rotation inducing surface 444 of insert 400.


In some cases, the epicondylar axis 242 (the line connecting the lateral epicondylar prominence and the medial sulcus of the medial epicondyle) could have a tendency to decline, which could cause rotation about the long axis of the femur and might cause laxity of the LCL. According to certain embodiments of the invention, it would be possible to keep the epicondylar axis 242 at the same height, by causing the sagittal curve of the posterior portion 224 of the lateral condyle 204 to be extended outwardly as could be visualized with reference to, for instance, FIGS. 4-11. For example, at 155° flexion, the lateral contact point 434 could decline approximately 2.6 mm, so that 2.6 mm would be added to the lateral condyle 204 thickness at a point corresponding to 155° flexion on the condyle to accomplish such a result, although other structures could be created to achieve the same end.


When assembled, the femoral component 200 shown in the drawings is positioned on the insert 400 so that there is a slight posterior overhang. This optimizes the anterior-posterior patella ligament force components. The overhang may be much less than in conventional knee prostheses. For example, in conventional knee prostheses, the posterior overhang of the femoral component 200 may be as much as 6 mm. However, in knee prosthesis according to certain embodiments and aspects of the invention, the posterior overhang of the femoral component 200 is approximately 2 mm.


As explained above, axial rotation is normal in knee joint motion. The “screw-home” mechanism is example of this motion. In the normal knee, during knee extension, the femur is positioned anteriorly on the tibial plateau. During the last 20° of knee extension, the femur glides anteriorly on the tibia and produces external tibial rotation. This screw-home mechanism in terminal extension results in tightening of both cruciate ligaments and locks the knee such that the tibia is in the position of maximal stability with respect to the femur.


When the normal knee begins to flex, posterior glide of the femur begins first on the lateral tibial surface. Between approximately 0° and 130° of flexion, posterior glide on the lateral side produces relative tibial internal rotation, a reversal of the screw-home mechanism.


Knee prostheses 100 according to certain embodiments of the invention incorporate an allowance that mimics the screw-home mechanism. The screw-home allowance may be achieved by incorporating a swept surface on the lateral surface 416 of the insert 400. The screw-home allowance is illustrated most clearly in FIG. 12. FIGS. 12-19 demonstrate that as the knee flexes from approximately zero degrees to approximately 130 degrees, the femoral component 200 and the insert 400 rotate relative to each other generally about a closely grouped set of medial contact points 436. As the knee flexes, the femoral component 200 rotates externally relative to the insert 400, which would be fixed on a tibial component 300 in a fully assembled knee prosthesis 100; or considered from the other perspective, the insert 400 and the tibia rotate internally relative to the femoral component 200 and the femur. The asymmetrical shape of the posterior cam 232 reduces force on the central post 422 that would oppose this rotation.


This rotation, along with the increased flexion of the knee prostheses 100 of the invention, is evident in the series of side views of portions of a knee prosthesis 100 shown in FIGS. 4-11. To demonstrate the rotation between the femoral component 200 and the insert 400, which would be fixed on a tibial component 300 in a fully assembled knee prosthesis 100, the insert 400 shown remains stationary, as the femoral component 200 rotates substantially about the medial contact point. Thus, as shown in FIG. 4, the knee is fully extended. As the knee flexes to 90 degrees (shown in FIG. 7), the lateral condylar section 204 of the femoral component 200 rotates posteriorly on the lateral side 416 of the insert 400. The rotation continues as the knee flexes to 130 degrees, as shown in FIG. 9, reaching at least approximately 8 degrees of internal rotation of the tibia relative to the femur. As the knee continues to flex beyond approximately 130 degrees, as shown in FIGS. 10-11, the internal rotation stays substantially the same, as the relative motion is primarily posterior translation of the femoral component on the insert.


As the drawings show, when the knee prosthesis 100 is assembled, the central post or raised portion of the insert 400 fits within the intercondylar recess. Because the femoral component 200 and the insert 400 are not fastened to each other, the femoral component 200 is able to easily articulate on the insert 400.



FIGS. 4-11 thus sequentially show, from a side cross sectional aspect, kinematics of components of a knee prosthesis according to a preferred embodiment of the invention. FIGS. 12-19 show the same kinematics from a plan aspect, looking “down” on the prosthesis. These figures show kinematics of the prosthesis components at flexion angles of 0, 30, 60, 90, 120, 130, 140, and 150 degrees, respectively. At flexion angles of approximately 50 to 60 degrees, the cam 232 begins contacting the post 422 for posterior stabilization, as shown in FIG. 6. As the rotation of the femoral component 200 continues, the patella implant 500 moves down the trochlear groove 206, which is structured according to aspects of the invention to simulate natural anatomy in order to allow the patella implant 500 to track properly, and generally from a lateral to medial position relative to the femoral component 200 as flexion continues. In this fashion, the shape of the femoral component accommodates the natural action of the kneecap as a fulcrum on the knee joint for the considerable forces applied by the quadriceps and the patellar ligament. As the knee flexes from substantially zero degrees of flexion to substantially 130 degrees of flexion, the tibial rotation inducing surface 444 of the particular (nonlimiting) structure shown in the drawings acting in combination with the lateral condylar section 204, plus the action of the asymmetrical posterior cam 232 of the femoral component 200 on the post 422 of the insert, impart inward rotation to the insert 400 relative to the femur. This inward rotation corresponds to such inward rotation in the normal knee, and allows, among other things, the lower leg to be “folded” inward relative to the upper leg so that the patellar ligament and tendons from the quadriceps are not forced to be extended over the lateral part of the knee as is the case in some conventional designs. Yet the structure of the components shown in these drawings allows such natural internal rotation and other natural articulation of the tibia and femur relative to each other without freeing rotation of the insert relative to the tibial implant, or freeing other components in the prosthesis to move relative to each other, thereby taxing the other, weaker ligaments and tendons forming part of the knee, which are required to assume the new task of restraining the freed prosthetic components.


Designs more closely approximating the structure and/or operation of the natural knee may be carried out according to the present invention by considering forces acting on the knee that are of more considerable magnitude than other forces. For instance, 6 major forces on the tibia can be used to simulate what a natural knee experiences during certain activities such as walking: (1) ground reaction force which can range from some part up to multiples of body weight in a normal knee kinetic environment; (2) tension imposed by the quadriceps acting through the patella tendon in a generally proximal direction tending to proximal-posterior in flexion and to proximal-anterior in extension; (3) tension applied by the hamstrings in a generally posterior direction; (4, 5) contact force of each condyle on its corresponding bearing surface of the tibial plateau; and (6) posterior stabilization force imposed by the posterior cruciate ligament or insert on the femur. The inventors have recognized that reducing the myriad of forces acting on the knee (such as from various more minor tendons and ligaments) to a manageable number, which may increase as time and processing power continue to evolve, allows for reliable and effective testing of proposed knee prosthesis designs, by accurately simulating what real knees experience. This manageable set of conditions may be combined with information that is known about the structure and the kinematics of natural knees to impose an essentially realistic test regime for computer testing and development of acceptable knee prosthetic designs.


Applying a testing regime using a manageable but essentially realistic set of conditions allows iterative proposal of a design, testing it for performance in virtual, automated fashion in a computer, modification of the proposed design to reduce negative performance characteristics and to enhance positive ones, and repeated iteration of these tasks until an acceptable design is reached. The developers may therefore accordingly proceed at least partially iteratively, using test conditions that simulate what a real knee joint experiences and how it performs in such an environment, rather than attempting to design the complicated knee prosthetic components in a deterministic fashion based on anecdotal information, observation of knee components being articulated in the operating room, or based on assumptions that can be static and not reflect the complexity of nature.


The foregoing is provided for disclosure of various embodiments, aspects and structures relating to the invention. Various modifications, additions and deletions may be made to these embodiments and/or structures without departing from the scope and spirit of the invention.

Claims
  • 1. A femoral component of a knee prosthesis comprising: (a) a distal portion comprising a distal medial condyle articular surface and a distal lateral condyle articular surface, the distal portion extending generally in an anterior to posterior direction between an anterior end and a posterior end of the distal portion, wherein the distal medial and lateral condylar articular surfaces continuously convexly curve from the anterior end to the posterior end of the distal portion;(b) an anterior portion extending generally in a distal to proximal direction away from the anterior end of the distal portion, the anterior portion comprising a trochlear groove, a medial side and a lateral side; and(c) a posterior portion extending generally in the distal to proximal direction away from the posterior end of the distal portion, the posterior portion comprising a posterior medial condyle articular surface and a posterior lateral condyle articular surface; wherein the lateral side of the anterior portion projects further in a posterior to anterior direction than the medial side of the anterior portion; andwherein the distal medial condyle articular surface projects further in a proximal to distal direction than the distal lateral condyle articular surface; andwherein the posterior portion further comprises a planar medial interior surface and a planar lateral interior surface, and wherein a thickness defined by the posterior medial condyle articular surface and the planar medial interior surface is greater than a thickness defined by the posterior lateral condyle articular surface and the planar lateral interior surface.
  • 2. The femoral component of claim 1, wherein the posterior medial condyle articular surface projects further in the anterior to posterior direction than the posterior lateral condyle articular surface.
  • 3. The femoral component of claim 1, wherein at least one of the distal, anterior and posterior portions further comprises a planar interior surface.
  • 4. The femoral component of claim 1, wherein the femoral component is configured for articulation with a tibial prosthetic component.
  • 5. The femoral component of claim 1, wherein at least the posterior portion defines an intracondylar notch extending between the posterior medial condyle articular surface and the posterior lateral condyle articular surface.
  • 6. The femoral component of claim 1, wherein the lateral side of the anterior portion is configured to act as a patellar buttress to guide the patella in flexion and extension.
  • 7. A femoral component of a knee prosthesis comprising: (a) a distal portion comprising a distal medial condyle articular surface and a distal lateral condyle articular surface, the distal portion extending generally in an anterior to posterior direction between an anterior end and a posterior end of the distal portion, wherein the distal medial and lateral condylar articular surfaces continuously convexly curve from the anterior end to the posterior end of the distal portion;(b) an anterior portion extending generally in a distal to proximal direction away from the anterior end of the distal portion, the anterior portion comprising a trochlear groove, a medial side and a lateral side; and(c) a posterior portion extending generally in the distal to proximal direction away from the posterior end of the distal portion, the posterior portion comprising a posterior medial condyle articular surface and a posterior lateral condyle articular surface; wherein the lateral side of the anterior portion projects further in a posterior to anterior direction than the medial side of the anterior portion; andwherein the posterior medial condyle articular surface projects further in the anterior to posterior direction than the posterior lateral condyle articular surface.
  • 8. The femoral component of claim 7, wherein at least one of the distal, anterior and posterior portions further comprises a planar interior surface.
  • 9. The femoral component of claim 7, wherein the posterior portion further comprises a planar medial interior surface and a planar lateral interior surface, and wherein a thickness defined by the posterior medial condyle articular surface and the planar medial interior surface is greater than a thickness defined by the posterior lateral condyle articular surface and the planar lateral interior surface.
  • 10. The femoral component of claim 7, wherein the femoral component is configured for articulation with a tibial prosthetic component.
  • 11. The femoral component of claim 7, wherein at least the posterior portion defines an intracondylar notch extending between the posterior medial condylar articular surface and the posterior lateral condylar articular surface.
  • 12. The femoral component of claim 7, wherein the lateral side of the anterior portion is configured to act as a patellar buttress to guide the patella in flexion and extension.
  • 13. A femoral component of a knee prosthesis comprising: (a) a distal portion comprising a distal medial condyle articular surface and a distal lateral condyle articular surface, the distal portion extending generally in an anterior to posterior direction between an anterior end and a posterior end of the distal portion, wherein the distal medial and lateral condylar articular surfaces continuously convexly curve from the anterior end to the posterior end of the distal portion;(b) an anterior portion extending generally in a distal to proximal direction away from the anterior end of the distal portion, the anterior portion comprising a trochlear groove, a medial side and a lateral side; and(c) a posterior portion extending generally in the distal to proximal direction away from the posterior end of the distal portion, the posterior portion comprising a posterior medial condyle articular surface and a posterior lateral condyle articular surface; wherein the lateral side of the anterior portion projects further in a posterior to anterior direction than the medial side of the anterior portion;wherein the distal medial condyle articular surface projects further in a proximal to distal direction than the distal lateral condyle articular surface; and wherein the posterior medial condyle articular surface projects further in the anterior to posterior direction than the posterior lateral condyle articular surface.
  • 14. The femoral component of claim 13, wherein at least one of the distal, anterior and posterior portions further comprises a planar interior surface.
  • 15. The femoral component of claim 13, wherein the posterior portion further comprises a planar medial interior surface and a planar lateral interior surface, and wherein a thickness defined by the posterior medial condyle articular surface and the planar medial interior surface is greater than a thickness defined by the posterior lateral condyle articular surface and the planar lateral interior surface.
  • 16. The femoral component of claim 13, wherein the femoral component is configured for articulation with a tibial prosthetic component.
  • 17. The femoral component of claim 13, wherein at least the posterior portion defines an intracondylar notch extending between the posterior medial condylar articular surface and the posterior lateral condylar articular surface.
  • 18. The femoral component of claim 13, wherein the lateral side of the anterior portion is configured to act as a patellar buttress to guide the patella in flexion and extension.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S Patent application Ser. No. 12/582,300 filed Oct. 20, 2009, which is a continuation application of U.S. Patent application Ser. No. 12/023,112 filed Jan. 31, 2008 now U.S. Pat. No. 7,922,771, which is a continuation application of U.S. Patent application Ser. No. 10/743,885 filed Dec. 22, 2003, now patented as U.S. Pat. No. 7,326,252, which application claims priority to U.S. Ser. No. 60/435,426 entitled “Knee Prosthesis Having Improved Stability and Rotational Control” filed Dec. 20, 2002, the entire contents of all of which are herein incorporated by this reference.

US Referenced Citations (307)
Number Name Date Kind
3748662 Helfet Jul 1973 A
3774244 Walker Nov 1973 A
3798679 Ewald Mar 1974 A
3816855 Saleh Jun 1974 A
3924277 Freeman et al. Dec 1975 A
3958278 Lee et al. May 1976 A
4016606 Murray et al. Apr 1977 A
4178641 Grundel et al. Dec 1979 A
4207627 Cloutier Jun 1980 A
4209861 Walker et al. Jul 1980 A
4213209 Insall et al. Jul 1980 A
4249270 Bahler et al. Feb 1981 A
4340978 Buechel et al. Jul 1982 A
4353135 Forte et al. Oct 1982 A
4358859 Schurman et al. Nov 1982 A
4474177 Whiteside Oct 1984 A
4524766 Petersen Jun 1985 A
4568348 Johnson et al. Feb 1986 A
4586933 Shoji et al. May 1986 A
4653488 Kenna et al. Mar 1987 A
4659331 Matthews et al. Apr 1987 A
4662889 Zichner et al. May 1987 A
4703751 Pohl Nov 1987 A
4711639 Grundel Dec 1987 A
4714472 Averill et al. Dec 1987 A
4714473 Bloebaum Dec 1987 A
4721104 Kaufman et al. Jan 1988 A
4722330 Russell et al. Feb 1988 A
4731086 Whiteside et al. Mar 1988 A
4770663 Hanslik et al. Sep 1988 A
4787383 Kenna Nov 1988 A
4822365 Walker et al. Apr 1989 A
4834758 Lane et al. May 1989 A
4926847 Luckman May 1990 A
4936853 Fabian et al. Jun 1990 A
4938769 Shaw Jul 1990 A
4944757 Martinez et al. Jul 1990 A
4950297 Ehoy et al. Aug 1990 A
4950298 Gustilo et al. Aug 1990 A
4963152 Hofmann et al. Oct 1990 A
4979949 Matsen, III et al. Dec 1990 A
5002547 Poggie et al. Mar 1991 A
5007933 Sidebotham et al. Apr 1991 A
5021061 Wevers et al. Jun 1991 A
5032134 Lindwer Jul 1991 A
5047057 Lawes Sep 1991 A
5053037 Lackey Oct 1991 A
5062852 Dorr et al. Nov 1991 A
5071438 Jones et al. Dec 1991 A
5080675 Lawes et al. Jan 1992 A
5092869 Waldron Mar 1992 A
5098436 Ferrante et al. Mar 1992 A
5100409 Coates Mar 1992 A
5116375 Hofmann May 1992 A
5122144 Bert et al. Jun 1992 A
5129909 Sutherland Jul 1992 A
5133758 Hollister Jul 1992 A
5133759 Turner Jul 1992 A
5147405 Van Zile et al. Sep 1992 A
5147406 Houston et al. Sep 1992 A
5176710 Hahn et al. Jan 1993 A
5181925 Houston et al. Jan 1993 A
5201881 Evans Apr 1993 A
5203807 Evans et al. Apr 1993 A
5219362 Tuke et al. Jun 1993 A
5226916 Goodfellow et al. Jul 1993 A
5228459 Caspari Jul 1993 A
5234433 Bert et al. Aug 1993 A
5236432 Matsen et al. Aug 1993 A
5236461 Forte Aug 1993 A
5250050 Poggie et al. Oct 1993 A
5263498 Caspari et al. Nov 1993 A
5282803 Lackey Feb 1994 A
5282867 Mikhail Feb 1994 A
5282870 Moser et al. Feb 1994 A
5304181 Caspari et al. Apr 1994 A
5314482 Goodfellow et al. May 1994 A
5326358 Aubriot et al. Jul 1994 A
5330532 Ranawat Jul 1994 A
5330533 Walker Jul 1994 A
5330534 Herrington et al. Jul 1994 A
5336267 Kubein-Meesenburg et al. Aug 1994 A
5358527 Forte Oct 1994 A
5358529 Davidson Oct 1994 A
5358531 Goodfellows et al. Oct 1994 A
5370699 Hood et al. Dec 1994 A
5370701 Finn Dec 1994 A
5405398 Buford, III et al. Apr 1995 A
5413604 Hodge May 1995 A
5417694 Marik et al. May 1995 A
5454816 Ashby Oct 1995 A
5470354 Hershberger et al. Nov 1995 A
5480443 Elias Jan 1996 A
5480446 Goodfellows et al. Jan 1996 A
5507820 Pappas Apr 1996 A
5514143 Bonutti et al. May 1996 A
5520695 Luckman May 1996 A
5549684 Amino et al. Aug 1996 A
5549686 Johnson et al. Aug 1996 A
5549688 Ries et al. Aug 1996 A
5556432 Kubein-Meesenburg et al. Sep 1996 A
5609645 Vinciguerra Mar 1997 A
5611802 Samuelson et al. Mar 1997 A
5639279 Burkinshaw et al. Jun 1997 A
5658342 Draganich et al. Aug 1997 A
5658344 Hurlburt Aug 1997 A
5667511 Vendrely et al. Sep 1997 A
5681354 Eckhoff Oct 1997 A
5682886 Delp et al. Nov 1997 A
5683468 Pappas Nov 1997 A
5690635 Matsen et al. Nov 1997 A
5690637 Wen et al. Nov 1997 A
5702458 Burstein et al. Dec 1997 A
5723016 Minns et al. Mar 1998 A
5728162 Eckhoff Mar 1998 A
5738686 Kubein-Meesenburg et al. Apr 1998 A
5741259 Chan Apr 1998 A
5755801 Walker et al. May 1998 A
5755803 Haines et al. May 1998 A
5755804 Schmotzer et al. May 1998 A
5766257 Goodman et al. Jun 1998 A
5776200 Johnson et al. Jul 1998 A
5782921 Colleran et al. Jul 1998 A
5782925 Collazo et al. Jul 1998 A
5800552 Forte Sep 1998 A
5810824 Chan Sep 1998 A
5810827 Haines et al. Sep 1998 A
5824100 Kester et al. Oct 1998 A
5824102 Buscayret Oct 1998 A
5824105 Ries et al. Oct 1998 A
5871545 Goodfellows et al. Feb 1999 A
5871546 Colleran et al. Feb 1999 A
5879392 McMinn Mar 1999 A
5906643 Walker May 1999 A
5935173 Roger et al. Aug 1999 A
5954770 Schmotzer et al. Sep 1999 A
5997577 Herrington et al. Dec 1999 A
6013103 Kaufman et al. Jan 2000 A
6039764 Pottenger et al. Mar 2000 A
6056779 Noyer et al. May 2000 A
6059788 Katz May 2000 A
6068658 Insall et al. May 2000 A
6080195 Colleran et al. Jun 2000 A
6086590 Margulies et al. Jul 2000 A
6099570 Livet et al. Aug 2000 A
6120543 Kubein-Meesenburg et al. Sep 2000 A
6123729 Insall et al. Sep 2000 A
6132468 Mansmann Oct 2000 A
6139581 Engh et al. Oct 2000 A
6156223 Sigel et al. Dec 2000 A
6165223 Metzger et al. Dec 2000 A
6171340 McDowell Jan 2001 B1
6190415 Cooke et al. Feb 2001 B1
6197064 Haines et al. Mar 2001 B1
6203576 Afriat et al. Mar 2001 B1
6205411 DiGiola et al. Mar 2001 B1
6206926 Pappas Mar 2001 B1
6210443 Marceaux et al. Apr 2001 B1
6235060 Kubein-Meesenburg et al. May 2001 B1
6264697 Walker Jul 2001 B1
6281264 Salovey et al. Aug 2001 B1
6306172 O'Neil et al. Oct 2001 B1
6325828 Dennis et al. Dec 2001 B1
6361564 Marceaux et al. Mar 2002 B1
6379388 Ensign et al. Apr 2002 B1
6406497 Takei Jun 2002 B2
6413279 Metzger et al. Jul 2002 B1
6428577 Evans et al. Aug 2002 B1
6436145 Miller 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
6500208 Metzger et al. Dec 2002 B1
6506215 Letot et al. Jan 2003 B1
6547790 Harkey, III et al. Apr 2003 B2
6554838 McGovern et al. Apr 2003 B2
6558426 Masini May 2003 B1
6569202 Whiteside May 2003 B2
6575980 Robie et al. Jun 2003 B1
6589283 Metzger et al. Jul 2003 B1
6620198 Burstein et al. Sep 2003 B2
6623526 Lloyd Sep 2003 B1
6645251 Salehi et al. Nov 2003 B2
6652587 Felt et al. Nov 2003 B2
6695848 Haines Feb 2004 B2
6702821 Bonutti Mar 2004 B2
6730128 Burstein May 2004 B2
6755864 Brack et al. Jun 2004 B1
6764516 Pappas Jul 2004 B2
6770097 Leclercq Aug 2004 B2
6770099 Andriacchi et al. Aug 2004 B2
6773461 Meyers et al. Aug 2004 B2
6811568 Minamikawa Nov 2004 B2
6827723 Carson Dec 2004 B2
6846329 McMinn Jan 2005 B2
6866683 Gerbec et al. Mar 2005 B2
6866684 Fell et al. Mar 2005 B2
6887276 Gerbec et al. May 2005 B2
6893467 Bercovy May 2005 B1
6902582 Kubein-Meesenburg et al. Jun 2005 B2
6911044 Fell et al. Jun 2005 B2
6916324 Sanford et al. Jul 2005 B2
6916340 Metzger et al. Jul 2005 B2
6960213 Chervitz et al. Nov 2005 B2
7018418 Amrich et al. Mar 2006 B2
7048741 Swanson May 2006 B2
7066963 Naegeri Jun 2006 B2
7077867 Pope et al. Jul 2006 B1
7104996 Bonutti Sep 2006 B2
7141053 Rosa et al. Nov 2006 B2
7160330 Axelson, Jr. et al. Jan 2007 B2
7275218 Petrella et al. Sep 2007 B2
7326252 Otto et al. Feb 2008 B2
7364590 Siebel Apr 2008 B2
7371240 Pinczewski et al. May 2008 B2
7615082 Naegeri et al. Nov 2009 B2
7922771 Otto et al. Apr 2011 B2
20010018615 Biegun et al. Aug 2001 A1
20010043918 Masini et al. Nov 2001 A1
20020032450 Trudeau et al. Mar 2002 A1
20020055784 Burstein et al. May 2002 A1
20020058997 O'connor et al. May 2002 A1
20020103541 Meyers et al. Aug 2002 A1
20020107576 Meyers et al. Aug 2002 A1
20020120340 Metzger et al. Aug 2002 A1
20020161447 Salehi et al. Oct 2002 A1
20020173852 Felt et al. Nov 2002 A1
20020177852 Chervitz et al. Nov 2002 A1
20020177853 Chervitz et al. Nov 2002 A1
20030009228 Meyers et al. Jan 2003 A1
20030009230 Gundlapalli et al. Jan 2003 A1
20030055494 Bezuidenhout et al. Mar 2003 A1
20030055501 Fell et al. Mar 2003 A1
20030055509 McCue et al. Mar 2003 A1
20030060882 Fell et al. Mar 2003 A1
20030060883 Fell et al. Mar 2003 A1
20030060884 Fell et al. Mar 2003 A1
20030060885 Fell et al. Mar 2003 A1
20030069591 Carson et al. Apr 2003 A1
20030093156 Metzger et al. May 2003 A1
20030100953 Rosa et al. May 2003 A1
20030153977 Suguro et al. Aug 2003 A1
20030153978 Whiteside Aug 2003 A1
20030153979 Hughes et al. Aug 2003 A1
20030163201 McMinn Aug 2003 A1
20030220697 Justin et al. Nov 2003 A1
20030225410 Chervitz et al. Dec 2003 A1
20030225458 Donkers et al. Dec 2003 A1
20040006393 Burkinshaw Jan 2004 A1
20040030387 Landry et al. Feb 2004 A1
20040034432 Hughes et al. Feb 2004 A1
20040044414 Nowakowski Mar 2004 A1
20040102852 Johnson et al. May 2004 A1
20040122522 Kubein-Meesenburg et al. Jun 2004 A1
20040143339 Axelson, Jr. et al. Jul 2004 A1
20040153066 Coon et al. Aug 2004 A1
20040153164 Sanford Aug 2004 A1
20040162620 Wyss Aug 2004 A1
20040193280 Webster et al. Sep 2004 A1
20040199249 Fell Oct 2004 A1
20040199250 Fell Oct 2004 A1
20040204766 Siebel Oct 2004 A1
20040249467 Meyers et al. Dec 2004 A1
20040249468 Suguro et al. Dec 2004 A1
20040267363 Fell et al. Dec 2004 A1
20050021147 Tarabichi Jan 2005 A1
20050033424 Fell Feb 2005 A1
20050055102 Tornier et al. Mar 2005 A1
20050107886 Crabtree et al. May 2005 A1
20050125069 Naegeri et al. Jun 2005 A1
20050143832 Carson Jun 2005 A1
20050171604 Michalow Aug 2005 A1
20050197710 Naegeri Sep 2005 A1
20050209701 Sugure et al. Sep 2005 A1
20050267476 Chervitz et al. Dec 2005 A1
20060015109 Haines Jan 2006 A1
20060015115 Haines Jan 2006 A1
20060015116 Haines Jan 2006 A1
20060015117 Haines Jan 2006 A1
20060030853 Haines Feb 2006 A1
20060030854 Haines Feb 2006 A1
20060030855 Haines Feb 2006 A1
20060030944 Haines Feb 2006 A1
20060052875 Bernero et al. Mar 2006 A1
20060058882 Haines Mar 2006 A1
20070078517 Engh et al. Apr 2007 A1
20080119940 Otto et al. May 2008 A1
20080154270 Haines et al. Jun 2008 A1
20090076514 Haines Mar 2009 A1
20090210066 Jasty Aug 2009 A1
20090319048 Shah et al. Dec 2009 A1
20090319049 Shah et al. Dec 2009 A1
20100042224 Otto et al. Feb 2010 A1
20100076567 Justin et al. Mar 2010 A1
20100100192 Haines et al. Apr 2010 A1
20100185203 Haines Jul 2010 A1
20110082559 Hartdegen et al. Apr 2011 A1
20110125280 Otto et al. May 2011 A1
20110125281 Otto et al. May 2011 A1
20110125282 Otto et al. May 2011 A1
20110125283 Otto et al. May 2011 A1
20110130842 Otto et al. Jun 2011 A1
20110130843 Otto et al. Jun 2011 A1
20110137426 Otto et al. Jun 2011 A1
20110137427 Otto et al. Jun 2011 A1
20110137619 Otto et al. Jun 2011 A1
Foreign Referenced Citations (71)
Number Date Country
3314038 Oct 1983 DE
19529824 Feb 1997 DE
0121142 Oct 1984 EP
0189253 Jul 1986 EP
0243109 Oct 1987 EP
0327249 Aug 1989 EP
0380451 Jan 1990 EP
0381352 Aug 1990 EP
0941719 Sep 1990 EP
0420460 Apr 1991 EP
0466659 Jan 1992 EP
0510299 Oct 1992 EP
0336774 Dec 1992 EP
0555003 Jan 1993 EP
0538153 Apr 1993 EP
0791338 Aug 1997 EP
0806920 Nov 1997 EP
0916321 May 1999 EP
0923916 Jun 1999 EP
0970667 Jan 2000 EP
0988840 Mar 2000 EP
1477143 Nov 2004 EP
2635675 Mar 1990 FR
2664157 Jan 1992 FR
2701387 Aug 1994 FR
2710258 Mar 1995 FR
2760352 Sep 1998 FR
1409150 Oct 1975 GB
2007980 Jul 1982 GB
2296443 Jul 1996 GB
2324249 Oct 1998 GB
2335145 Sep 1999 GB
61170453 Aug 1986 JP
62133948 Jun 1987 JP
62254750 Nov 1987 JP
02246971 Oct 1990 JP
0315460 Jan 1991 JP
04297254 Oct 1992 JP
05041510 Jun 1993 JP
06237941 Aug 1994 JP
11504226 Feb 1996 JP
2001524349 Jun 1999 JP
11313845 Nov 1999 JP
2000116682 Apr 2000 JP
2000201955 Jul 2000 JP
2000312691 Nov 2000 JP
2002224149 Aug 2002 JP
2121319 Nov 1998 RU
WO9110408 Jul 1991 WO
WO9303681 Mar 1993 WO
WO9322990 Nov 1993 WO
WO9325157 Dec 1993 WO
WO9405212 Mar 1994 WO
WO9409730 May 1994 WO
WO9422397 Oct 1994 WO
WO9428812 Dec 1994 WO
WO9503003 Feb 1995 WO
WO9601087 Jan 1996 WO
WO9601588 Jan 1996 WO
9603939 Feb 1996 WO
WO9603097 Feb 1996 WO
WO9623460 Aug 1996 WO
WO9624311 Aug 1996 WO
WO9729703 Aug 1997 WO
WO9729704 Aug 1997 WO
WO9820817 May 1998 WO
9927872 Jun 1999 WO
WO9927872 Jun 1999 WO
WO9930649 Jun 1999 WO
WO0113825 Mar 2001 WO
WO2004100839 Nov 2004 WO
Non-Patent Literature Citations (94)
Entry
‘European Hospital . . . The European Forum for Those in the Business of Making Healthcare Work,’ 12(5/03):1-24 (Oct./Nov. 2003).
Whiteside Ortholoc Total Knee System: Surgical Procedure, Dow Corning Wright, pp. WMT000001-WMT000040, Jun. 1985.
Zimmer, Insall/Burstein II Constrained Condylar: Modular Knee System, Surgical Technique, copyright 1989.
Zimmer, The Miller/Galante Advantage: Total Knee System, pp. ZH000156953-ZH000156968.
Whiteside Ortholoc Total Knee System, Dow Corning Wright, pp. ZH000109679-ZH000109690.
Zimmer, Insall/Burnstein II, Modular Knee System, Surgical Technique, pp. ZH000109691-ZH000109710.
Exhibits 4, 5 and 8 from Hudson Surgical Design, Inc. v. Zimmer Holdings, Inc., Zimmer Inc., Rush System for Health and Rush University Medical Center, Hudson Surgical Design, Inc.'s Opening Brief on Claim Construction Case No. 1:08-cv-01566, Civil Action No. 08C1566, Document No. 83, filed Nov. 17, 2008, 6 pages.
Hudson Surgical Design v. Zimmer Holdings, Inc., et al., Revised Final Claim Construction Chart, filed Mar. 11, 2009, 18 pages.
Haines et al., Accelerated Examination Search Statement and Support Document for Femoral Prosthetic Implant from U.S. Appl. No. 12/638,692, dated Dec. 15, 2009, 85 pages.
Office Action for U.S. Appl. No. 12/638,692, mailed Oct. 22, 2010, 19 pages.
Supplemental Information Disclosure Statement filed in U.S. Appl. No. 12/638,692, Nov. 16, 2010, 19 pages.
Haines et al., Correct Accelerated Examination Search Statement and Support Document for Femoral Prosthetic Implant from U.S. Appl. No. 12/757,778 dated Apr. 9, 2010, 104 pages.
Office Action for U.S. Appl. No. 11/933,298, mailed Dec. 2, 2010, 20 pages.
Freeman, Samuelson, Total Knee System, Biomet, Inc., 1994, attached as Exhibit F, 60 pages.
Freeman, M.A.R., and Samuelson, K.M., Protek® Mark II Total Knee Replacement System, published 1985, 21 pages, attached as Exhibit G.
Protek F/S Modular Total Knee Replacement System, published by Protek, Jan. 1991, pp. 1-58, attached as Exhibit H.
Buechel, F.F., et al., “Low Contact Stree Meniscal Bearing Unicompartmental Knee Replacement : Long-Term Evaluation of Cemented and Cementless Results,” Journal of Orthopaedic Rheumatology, presented at the 57th Annual American Academy of Orthopaedic Surgeons Meeting, New Orleans, LA, Feb. 11, 1990, Bates No. DEP00004096-DEP00004107, 13 pages.
N.J. Unicompartmental Knee, Sep. 15, 1989, Bates No. DEP00004108-DEP00004116, 10 pages.
Buechel, F.F., “NJ LCS Unicompartmental Knee System with Porocoat: Surgical Procedure,” Oct. 24, 1994, Bates No. DEP00004117-DEP00004130, 15 pages.
Buechel, F.F., NJ LCS Unicompartmental Knee System with Proocoat, 1994, Bates No. DEP00004142-DEP4152, 11 pages.
Engh, G.A., et al., “The AMK Total Knee System, Design Rationale and Surgical Procedure,” Published by DePuy, 1989, Bates No. DEP00004153-DEP00004201, 50 pages.
Chapman, Michael, W., ed., “Primary Total Knee Arthroplasty,” Operative Orthopaedics, vol. 1, published by J.B. Lippincott Co., Philadelphia, 1988, pp. 719-725 and p. 86, Bates No. DEP00004236-DEP00004247.
Crossett, L.S., et al., ‘AMK Congruency Instrument System, Surgical Technique,’ published by DePuy, 1997, Bates No. DEP00004252-DEP00004267, 17 pages.
Engh, G.A., et al., ‘AMK Surgical Technique,’ published by DePuy, 1989, Bates No. DEP00004299-DEP00004329, 32 pages.
Desjardins, D., et al., ‘Interax Operative Techniques,’ Interax, 1994, Bates No. DEP00004391-DEP00004411, 22 pages.
Desjardins, D., et al., ‘Interax Total Knee Operative Technique,’ Interax, 1993, Bates No. DEP00004412-DEP00004432, 22 pages.
Baird, et al., 'LCS Uni : Unicompartmental Knee System with Porocoat,>> published by DePuy, 1991, Bates No. DEP00004452-DEP00004462, 12 pages.
Oxford Meniscal Knee Phase II Unicompartmental Replacement, published by Biomet prior to Jun. 7, 1994, Bates No. DEP00004509-DEP00004515, 8 pages.
Scott, R.D., et al., ‘P.F.C. Signa Uni-compartmental Knee System,’ published by Johnson & Johnson, 1998, Bates No. DEP00004531-DEP00004539, 10 pages.
Scott, R.D., et al., ‘Unicondylar Unicompartmental Replacement for Osteoarthritis of the Knee,’ Journal of Bone and Joint Surgery, vol. 63-A, No. 4, Apr. 1, 1981, pp. 536-544, Bates No. DEP00004764-DEP00004775.
Office Action for U.S. Appl. No. 12/757,778, mailed Nov. 15, 2010, 17 pages.
U.S. Appl. No. 12/952,648, filed Nov. 23, 2010.
U.S. Appl. No. 12/952,625, filed Nov. 23, 2010.
U.S. Appl. No. 12/952,584, filed Nov. 23, 2010.
U.S. Appl. No. 12/952,779, filed Nov. 23, 2010.
U.S. Appl. No. 12/952,859, filed Nov. 23, 2010.
U.S. Appl. No. 12/952,611, filed Nov. 23, 2010.
U.S. Appl. No. 12/952,704, filed Nov. 23, 2010.
U.S. Appl. No. 12/971,623, filed Dec. 17, 2010.
U.S. Appl. No. 12/971,507, filed Dec. 17, 2010.
Ad-hoc press release Oct. 2, 2002, 2 pages http://www.aap.de/VirtuelleHosts/aap/en/Investor/News/Newsarchiv—2002/AH—02.10.2002 Accessed Jun. 13, 2006.
Mebio Knee, one page, 2006 http://www.aap.de/en/Produkte/Endoprothetik/Knieendoprothetic/Mebio—Knie/index—html Accessed Jun. 13, 2006.
Essinger, et al., “A Mathematical Model for the Evaluation of the Behaviour During Flexion of Condylar-Type Knee Prosthesis,” J. Biomechanics, 22:1229-1241 (1989).
Stiehl, et al., “In Vivo Kinematic Analysis of a Mobile Bearing Total Knee Prosthesis,” Clinical Orthopaedics and Related Research, 345:60-66 (1997).
Kim, et al., “Rollback in Porterior Cruciate Ligament-retaining Total Knee Arthroplasty,” The Journal of Arthroplasty, 12(5):553-561 (1997).
Matsuda, et al., “Knee Kinematics of Posterior Cruciate Ligament Sacrificed Total Knee Arthroplasty,” Clinical Orthopaedics and Related Research, 341:257-266 (1997).
Szivek, et al., “Average and Peak Contact Stress Distribution Evaluation of Total Knee Arthroplasties,” The Journal of Arthroplasty, 11(8):952-963 (1996).
Dennis, et al., “In Vivo Knee Kinematics Derived Using an Inverse Perspective Technique,” Clinical Orthopaedics and Related Research, 331:107-117 (1996).
Sathasivam, et al., “Optimization of the Bearing Surface Geometry of Total Knees,” J. Biomechanics, 27(3):255-264 (1994).
Office Action dated Oct. 27, 2009 in parent U.S. Appl. No. 12/023,112.
Response dated Mar. 1, 2010 in parent U.S. Appl. No. 12/023,112.
Office Action dated May 10, 2010 in parent U.S. Appl. No. 12/023,112.
Response dated Aug. 4, 2010 in parent U.S. Appl. No. 12/023,112.
Notice of Allowance dated Dec. 17, 2010 in parent U.S. Appl. No. 12/023,112.
Notice of Allowance dated Feb. 16, 2010 in parent U.S. Appl. No. 12/023,112.
Australian Office Action dated Oct. 14, 2011 in related Application No. 2010200901.
Office Action dated Apr. 18, 2011 in related U.S. Appl. No. 12/582,300.
Office Action dated Mar. 27, 2007 in related U.S. Appl. No. 10/743,885.
Notice of Allowance dated Sep. 13, 2007 in related U.S. Appl. No. 10/743,885.
Office Action dated Aug. 11, 2011 in related U.S. Appl. No. 12/582,300.
Office Action dated Aug. 19, 2011 in related U.S. Appl. No. 12/952,779.
Office Action dated Aug. 25, 2011 in related U.S. Appl. No. 12/952,859.
Office Action dated Aug. 17, 2011 in related U.S. Appl. No. 12/952,611.
Office Action dated Aug. 17, 2011 in related U.S. Appl. No. 12/952,704.
Office Action dated Aug. 11, 2011 in related U.S. Appl. No. 12/952,648.
Office Action dated Aug. 17, 2011 in related U.S. Appl. No. 12/952,625.
Office Action dated Jun. 7, 2011 in related U.S. Appl. No. 12/952,584.
Response dated Oct. 7, 2011 in related U.S. Appl. No. 12/952,584.
Office Action dated Sep. 16, 2011 in related U.S. Appl. No. 12/971,623.
Office Action dated Oct. 24, 2011 in related U.S. Appl. No. 12/971,507.
Office Communication dated Mar. 21, 2012 in related European Patent Application No. 10012160.7.
Office Action dated Dec. 21, 2011 in related Australian Patent Application No. 2010200901.
Office Action dated Jun. 19, 2012 in related Japanese Application No. 2010-152060.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/952,648.
Office Action dated Jul. 10, 2012 in U.S. Appl. No. 12/952,625.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/952,584.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/971,507.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/971,623.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/952,611.
Office Action dated Jul. 5, 2012 in U.S. Appl. No. 12/582,300.
Office Action dated Jul. 3, 2012 in U.S. Appl. No. 12/952,779.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/952,859.
Office Action dated Jul. 20, 2012 in U.S. Appl. No. 12/952,704.
Office Action dated Nov. 9, 2012 in U.S. Appl. No. 12/952,625.
Office Action dated Nov. 5, 2012 in U.S. Appl. No. 12/952,779.
Office Action dated Nov. 1, 2012 in U.S. Appl. No. 12/952,859.
Notice of Allowance dated Nov. 8, 2012 in U.S. Appl. No. 12/952,584.
Notice of Allowance dated Nov. 23, 2012 in U.S. Appl. No. 12/582,300.
Corrected Notice of Allowance dated Jan. 9, 2013 in U.S. Appl. No. 12/582,300.
Notice of Allowance dated Dec. 14, 2012 in U.S. Appl. No. 12/952,704.
Notice of Allowance dated Nov. 30, 2012 in U.S. Appl. No. 12/952,648.
Office Action dated Jan. 16, 2013 in U.S. Appl. No. 12/971,507.
Notice of Allowance dated Jan. 22, 2013 in U.S. Appl. No. 12/952,611.
Office Action dated Jan. 22, 2013 in U.S. Appl. No. 12/971,623.
Related Publications (1)
Number Date Country
20110130841 A1 Jun 2011 US
Provisional Applications (1)
Number Date Country
60435426 Dec 2002 US
Continuations (3)
Number Date Country
Parent 12582300 Oct 2009 US
Child 12952667 US
Parent 12023112 Jan 2008 US
Child 12582300 US
Parent 10743885 Dec 2003 US
Child 12023112 US