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.
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.
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
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
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
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
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
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
Certain embodiments of the femoral component 200 may include a posterior cam 232 as shown in
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
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
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
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,
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
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
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.
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.
This application is a continuation application of U.S patent application Ser. No. 12/582,300 filed Oct. 20, 2009 now U.S. Pat. No. 8,398,715, 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.
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 | Mikhall | 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 | DiGola 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 |
8066776 | O'Connor et al. | Nov 2011 | B2 |
8394147 | Otto et al. | Mar 2013 | B2 |
8394148 | Otto et al. | Mar 2013 | B2 |
8398715 | Otto et al. | Mar 2013 | B2 |
8398716 | Otto et al. | Mar 2013 | B2 |
8403992 | Otto et al. | Mar 2013 | B2 |
8425617 | Otto et al. | Apr 2013 | 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 |
20110125283 | Otto et al. | May 2011 | A1 |
20110130841 | Otto et al. | Jun 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 |
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 |
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, on 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. 12/952,667, filed Nov. 23, 2010. |
U.S. Appl. No. 12/952,779, 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. |
Office Action dated Aug. 11, 2011 in related U.S. Appl. No. 12/582,300. |
Office Action dated Aug. 17, 2011 in related U.S. Appl. No. 12/952,667. |
Office Action dated Aug. 19, 2011 in related U.S. Appl. No. 12/952,779. |
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. |
Australian Office Action dated Oct. 14, 2011 in related Application No. 2010200901. |
Office Action dated Apr. 18, 2011 in related U.S. Appl. No. 12/282,300. |
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 Dec. 21, 2011 in related Australian Application No. 2010200901. |
Office Communication dated Mar. 21, 2012 in related European Patent Application No. 10012160.7. |
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. 10, 2012 in U.S. Appl. No. 12/952,667. |
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. 12/952,704. |
Office Action dated Nov. 9, 2012 in U.S. Appl. No. 12/952,625. |
Notice of Allowance dated Nov. 8, 2012 in U.S. Appl. No. 12/952,667. |
Office Action dated Nov. 5, 2012 in U.S. Appl. No. 12/952,779. |
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. |
Notice of Allowance dated Feb. 14, 2013 in U.S. Appl. No. 12/952,779. |
Office Action dated May 13, 2013 in U.S. Appl. No. 12/952,625. |
Office Action dated May 24, 2013 in U.S. Appl. No. 12/971,507. |
Number | Date | Country | |
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20110125282 A1 | May 2011 | US |
Number | Date | Country | |
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60435426 | Dec 2002 | US |
Number | Date | Country | |
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Parent | 12582300 | Oct 2009 | US |
Child | 12952859 | US | |
Parent | 12023112 | Jan 2008 | US |
Child | 12582300 | US | |
Parent | 10743885 | Dec 2003 | US |
Child | 12023112 | US |