Abstract: A method for preoperatively characterizing an individual patient's biomechanic function in preparation of implanting a prosthesis is provided. The method includes subjecting a patient to various activities, recording relative positions of anatomy during said various activities, measuring force environments responsive to said patient's anatomy and affected area during said various activities, characterizing the patient's biomechanic function from said relative positions and corresponding force environments, inputting the measured force environments, relative positions of knee anatomy, and patient's biomechanic function characterization into one or more computer simulation models, inputting a computer model of the prosthesis into said one or more computer simulation models, and manipulating the placement of the prosthesis in the computer simulation using said patient's biomechanic function characterization and said computer model of the prosthesis to approximate a preferred biomechanical fit of the prosthesis.

Abstract: An implant for installation into a portion of an articular surface includes a protrusion configured to cover an un-excised portion of articular surface proximate to the implant. Another implant may form a cavity to allow the un-excised portion of articular surface to remodel over a perimeter edge of the implant. The implant may also include indentations such as grooves to promote articular cartilage remodeling over a portion of the load bearing surface of the implant. An elongated or non-round implant is also provided having two opposing concentric arcuate shaped sides, as well as a method to seat such an implant in an articular surface. A method for seating an implant without cutting articular cartilage is also provided.

Abstract: An implant for installation into a portion of an articular surface includes an implant shell component having a proximal load bearing wall with an outer proximal load bearing surface. A peripheral rim extending distally relative to the load bearing wall may provide a bone-facing distal pocket on the shell component. An inner implant component may be received in the bone-facing distal pocket of the implant such that a proximal surface of the inner component is spaced apart from a distal surface of the load bearing wall. The contour of the load bearing surface may be based on an original surface contour of an articular surface, and the load bearing wall of the shell component may be a deflectable wall, so that the load bearing surface can deflect under an applied load. The space between the load bearing wall and the inner implant may include a compressible fluid such as elastomeric gels.

Abstract: A femoral component for a knee prosthesis comprises a reduced wear polyethylene (RWPE). Preferably all of the femoral component is the RWPE and/or at least one condylar surface of the femoral component is the RWPE. The use of RWPE instead of conventional metal components reduces or eliminates complications associated with the use of metal such as fracture (mostly at the area of the bone-metal interface), mechanical failure, and metallosis. Use of the RWPE gives a prosthesis with long life, especially with respect to wear of the femoral component.

Abstract: A tear and fatigue resistant gel article comprising two or more communicating internal volumes like cavities when depressed by external pressure or force is capable of collapsing unto itself in a controllable and directionally preselected manner by venting static air within said internal through openings in said gel article, said gel article is made from gel compositions having rigidity of from about 20 gram Bloom to about 1,800 gram Bloom suitable for cushioning and other uses.

Abstract: Apparatus for driving current in a power circuit of a medical device inserted into a body of a subject includes a power transmitter, which is adapted to generate, in a vicinity of the body, an electromagnetic field having a predetermined frequency capable of inductively driving the current in the power circuit. A passive energy transfer amplifier, having a resonant response at the frequency of the electromagnetic field is placed in proximity to the medical device so as to enhance the current driven in the power circuit by the electromagnetic field.

Abstract: A composition, a medical implant constructed from the composition, and a method of making the composition are described. The composition is a composite material, comprising a porous, reticulated, open cell network having at least part of its surface coated with blue-black or black oxidized zirconium.

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

Abstract: An orthopaedic prosthesis includes a tibial bearing and a femoral component configured to articulate with the tibial bearing. The tibial bearing and the femoral component are configured to promote outward axial rotation of the femoral component with respect to the tibial component during knee flexion.

Abstract: A material comprising: from 98-50% by volume of zirconia as a matrix, which is stabilized with i) either of from about 2 to about 3 mole percent of yttria ii) or of from about 10 to about 15 mole percent of ceria; iii) or a mixture of ceria and yttria in the range of amounts as given in i) and ii) the stabilizing oxides may be substituted against each other in a ratio from 1:99 to 99:1 and a maximum stabilization of 3 mole percent related to pure yttria and 15 mole percent related to pure ceria respectively are not exceeded, and wherein the term mole percent is related to the zirconia matrix and wherein the zirconia matrix is obtainable from a) a powder of particles of zirconia having a mean particle size of <0.

Abstract: An improved method of performing surgery on a joint in a patient's body, such as a knee, includes making an incision in a knee portion of one leg while a lower portion of the one leg is extending downward from an upper portion of the one leg and while a foot connected with the lower portion of the one leg is below a support surface on which the patient is disposed. The incision is relatively short, for example, between seven and thirteen centimeters. A patella may be offset from its normal position with an inner side of the patella facing inward during cutting of a bone with a cutting tool. During cutting of the bone, one or more guide members having opposite ends which are spaced apart by a distance less than the width of an implant may be utilized to guide movement of a cutting tool.

Abstract: Highly crystalline, oxidation resistant crosslinked polymeric materials such as crosslinked ultrahigh molecular weight polyethylenes having high wear resistance, enhanced stiffness, enhanced tensile strength, a high level of fatigue and crack propagation resistance, and enhanced creep resistance can be manufactured by the new methods described herein.

Abstract: Systems and methods for providing deeper knee flexion capabilities, more physiologic load bearing and improved patellar tracking for knee prosthesis patients. Such systems and methods include (i) adding more articular surface to the antero-proximal posterior condyles of a femoral component, including methods to achieve that result, (ii) modifications to the internal geometry of the femoral component and the associated femoral bone cuts with methods of implantation, (iii) asymmetrical tibial components that have an unique articular surface that allows for deeper knee flexion than has previously been available, (iv) asymmetrical femoral condyles that result in more physiologic loading of the joint and improved patellar tracking and (v) modifying an articulation surface of the tibial component to include an articulation feature whereby the articulation pathway of the femoral component is directed or guided by articulation feature.

Abstract: Where a prosthetic joint component part has a relatively sharp edge which potentially can contact and thereby irritate or injure soft tissue juxtaposed with the component part at an implant site during articulation of the prosthetic joint, such as a posterior cruciate ligament juxtaposed with a component part of a prosthetic knee, the component part is provided with a deflector located, configured, dimensioned and directed for deflecting the soft tissue away from contact with the sharp edge during articulation of the prosthetic joint.

Abstract: A fixed-bearing prosthesis includes a femoral component having a medial condyle surface and a lateral condyle surface. The knee prosthesis also includes a bearing having a medial bearing surface configured to articulate with the medial condyle surface of the femoral component, and a lateral bearing surface configured to articulate with the lateral condyle surface of the femoral component. A tibial tray is secured to the bearing. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A posterior buttress extends along a posterior section of the perimeter of the tray's platform, and an anterior buttress extends along an anterior section of the perimeter of the tray's platform. Differently-sized tibial trays are interchangeable with differently-sized bearings.

Abstract: An implant for installation into a portion of an articular surface includes a protrusion configured to cover an un-excised portion of articular surface proximate to the implant. Another implant may form a cavity to allow the un-excised portion of articular surface to remodel over a perimeter edge of the implant. The implant may also include indentations such as grooves to promote articular cartilage remodeling over a portion of the load bearing surface of the implant. An elongated or non-round implant is also provided having two opposing concentric arcuate shaped sides, as well as a method to seat such an implant in an articular surface. A method for seating an implant without cutting articular cartilage is also provided.

Abstract: A femoral knee prosthesis system for resurfacing a resected articular surface at the distal end of a femur includes a femoral component adapted to mate with the resected articular surface; and an attachment member. The interior surface of the femoral component is configured to connect to the first attachment member when the femoral component is mated on the resected articular surface of the femur and when the first attachment member is passed through the medial side or the lateral side of the resected articular surface. The femoral component is available in one-piece and two-piece systems. Mating femoral components (e.g., tapered or with lips that interlock with grooves) are also disclosed.

Abstract: Method for selecting one or several knee prosthesis elements, by acquiring spatial data concerning spacing and tensioned femorotibial position, including the corresponding HKA angle, for at least three angular positions, of 20°, of 0°, and of the order of 90° in flexion, processing the data thus obtained to verify whether the HKA angles are substantially equal and included within the tolerable limits, and processing the data, in particular those corresponding to extension and flexion of 90° to determine the dimensions and/or positions of the implant.

Abstract: A tibial component of an artificial knee joint is provided which cooperates with a femoral component to allow pivoting rotation of the artificial knee joint in either a clockwise or counterclockwise direction. The tibial component includes a plate with a tapered dovetail rib thereon which allows an insert to be removably secured thereto to act as a meniscal structure for the tibial component. The insert has a proximal surface with left and right wells therein that include valleys to guide rotation of one condylar leg of a femoral component while holding a second condylar leg of the femoral component within the other one of the wells, allowing pivoting rotation in either direction. A nesting of the insert into a portion of the plate minimizes an overall height of the tibial component and minimizing tibial bone resection, while providing a greater resistance to shear forces upon the knee joint.

Abstract: An instrumented joint trial has a polymer layer defining a curved contoured articulating surface. A curved contoured sensor array is positioned below the polymer layer. Other components of the joint trial, such as a body with a proximal curved contoured surface, are positioned below the sensor array. The device can be made by forming a sheet of the polymer over the curved contoured surface of the joint trial body and then adhering the sensor array to one curved contoured surface of the formed polymer. The sensor array conforms to the shape of the formed polymer layer. The system includes a mating joint trial. The device may be used by temporarily attaching the joint trial to a resected portion of bone and then articulating the joint with the instrumented trial in place.

Abstract: A anteromedial approach to arthroplasty on a knee joint of a patient. The method of arthroplasty includes an arthrotomy that includes dissecting from medial to the tibial tubercle and around the medial border of the patella and up to the proximal border of the patella.

Abstract: An artificial joint as an endoprosthesis for a human joint, has at least two joint parts wherein each joint part has two functional surfaces that operatively interact with each other, one associated with the first joint part and the other with the second joint part. The two functional surfaces of each joint part are spheroidal in shape and convex-concave, concave-convex or convex-convex in shape in the proximal-distal arrangement, and the functional surfaces can each pivot around a pivoting axis. In order to create an artificial joint as an endoprosthesis for a human joint, whose motion behavior is perceptibly improved for the patient, the two pivoting axes of the two functional surfaces of each joint part are slanted towards each other.

Abstract: The invention concerns article having a surface oxide layer up to 20 nm thick, the surface oxide layer comprising chromium and cobalt oxides where the atomic ratio of Cr/Co is more than 3. The invention also concerns methods for treating a chromium containing material, said method comprising contacting said material with a gas plasma under conditions effective to oxidize at least a portion of the material; and contacting said material with an acid. The treated surface is corrosion resistant and can be used in orthopedic implants, especially the wear surface of the orthopedic implant to reduce wear, and other corrosive environment.

Abstract: An endoprothetical connection element for creating a knee arthrodesis comprises a coupling element that comprises a first fastener and a second fastener. The first fastener is adapted for connection with a first fastening element corresponding to the first fastener that is provided at a shaft insertable into a femur of a patient. The second fastener is adapted for connection with a second fastening element corresponding to the second fastener that is provided at a shaft insertable into a tibia of the patient. The coupling element is formed such that a first longitudinal axis of the femoral shaft connected to the first fastener and a second longitudinal axis of the tibial shaft connected to the second fastener include an angle different from 180 degrees which, when implanted into the body of the patient, is lying in a coronal plane of the patient.

Abstract: A device for use in connection with a bone, comprising a first surface and a second surface spaced apart from each other at a predetermined distance and angled relative to each other along a portion thereof. The device having a first ridge projecting from the first surface in a direction away from the second surface, the first ridge extending substantially along a length of the first surface, and a second ridge projecting from the second surface in a direction away from the first surface, the second ridge extending substantially along a length of the second surface in a direction substantially parallel to the first ridge. The device further includes a remote surface positioned more distant from the center of a bone, a proximate surface positioned more near the center of a bone, a fixed end surface, and a removable end surface extending in a first direction.

Abstract: Knee prosthesis for implanting in a knee joint has a femoral component, a tibial component and a hinge connecting the femoral component and the tibial component. The femoral component rotates around the transverse axis passing through center of the hinge and the center of rotation of the femoral component moves substantially along proximal-distal axis upon flexion of the knee joint.

Abstract: A system for cooperating with an elongated IM member during preparation of a bone for receiving a prosthesis can include a scaffold, skeleton or frame. An alignment assembly can be selectively coupled to the frame. The alignment assembly can cooperate with the IM member to position the frame relative to the bone. A cutting block can be selectively coupled to the frame. According to other features, a posterior stabilized (PS) box guide assembly can have a PS box guide attachment portion that selectively couples with the first attachment portion of the frame. A posterior foot can selectively couple with a second attachment portion on the frame. The posterior foot can be positioned to occupy space of a joint line in an installed position.

Abstract: An artificial joint associated with an implant having a pair of three dimensional and structurally extending bones, each defining a contoured and opposing end face and collectively defining a joint location. A plasticized layer is applied to an end face of each bone and coacts in substantially frictional reducing fashion with an opposing end face of a further selected bone. The plasticized layer further includes at least a plurality of projecting contact locations, between which are defined a network of valleys for receiving, supporting, and distributing a lubricant across a surface area associated with the layer.

Abstract: A femoral prosthesis may be formed as a femoral component incorporating a base material and an articulating material. In one exemplary embodiment, the base material is a metal and the articulating material is a polymer. Specifically, the base material provides strength and rigidity to the femoral component, while the articulating material contacts a tibial prosthesis or natural tibia during joint articulation. In one exemplary embodiment, the articulating material forms the articulating surface of one or more condyle portions of the femoral component.

Abstract: A modular knee system having various distal posterior femoral components that are interchangeable with each other and with various patellar-femoral joint components. Preferably, the modular knee system has a variety of components that are interchangeable and connectable to resurface the distal femur using either a unicompartmental femoral knee prosthesis or a bicompartmental femoral knee prosthesis. These components include a medial distal posterior femoral component, a lateral distal posterior femoral component, a patellar-femoral joint component, and an interconnection mechanism to modularly connect the components together.

Abstract: An orthopaedic implant includes a knee prosthetic component, adaptor, and stem extension. The adaptor includes a first mounting end and a second mounting end. The first mounting end is coupled to the knee prosthetic component, and the second mounting end is coupled to the stem extension. The first mounting end of the adaptor defines a first axis, and the second mounting end of the adaptor defines a second axis. The first axis is offset from and parallel to the second axis when viewed in a first anatomical plane. Additionally, the first axis and second axis define an angle therebetween when viewed in a second anatomical plane. In some embodiments, the second mounting end may be movable with respect to the first mounting end. In other embodiments, the adaptor may be integral with the stem extension. Additionally, in some embodiments, the adaptor may be embodied as multi-piece adaptor.

Abstract: A fixed-bearing prosthesis includes a femoral component having a medial condyle surface and a lateral condyle surface. The knee prosthesis also includes a bearing having a medial bearing surface configured to articulate with the medial condyle surface of the femoral component, and a lateral bearing surface configured to articulate with the lateral condyle surface of the femoral component. A tibial tray is secured to the bearing. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A posterior buttress extends along a posterior section of the perimeter of the tray's platform, and an anterior buttress extends along an anterior section of the perimeter of the tray's platform. Differently-sized tibial trays are interchangeable with differently-sized bearings.

Abstract: A knee joint prosthesis including a femoral component for attachment to a femur. The femoral component includes an anterior portion, first and second condylar portions extending from the anterior portion and having first and second bearing surfaces, the first and second condylar portions having first and second posterior ends, and a third condylar portion defined between the first and second condylar portions and extending anteriorly beyond the first and second posterior ends.

Abstract: A prosthetic device having a generally fixed member formed from a low friction material such as ultra-high molecular weight polyethylene and an articulating titanium member, which includes an articular bearing surface. The articular surface is a zirconium oxide layer formed by applying a coating of zirconium onto the titanium member and heating this in an oxygen-containing environment. This causes the zirconium to oxidize and further causes the zirconium to migrate into the titanium member forming a titanium zirconium diffusion layer, which prevents delamination.

Abstract: An artificial joint as an endoprosthesis for a human joint, including a first joint part having two first functional surfaces, a second joint part having two second functional surfaces, the two first and second functional surfaces of each joint part being convex-concave, concave-convex, or convex-convex in a proximal-distal direction, a projection associated with the first joint part; and a recess associated with the second joint part. The recess is configured to engage with the projection so as to determine a relative position of the first and second joint parts in a transverse plane of the joint and to form a stop for a sliding movement of the first and second joint parts relative to each other. The two first functional surfaces are pivotable about a pivot axis with respect to the second functional surfaces and each of the first functional surfaces rolls and slides with respect to the second functional surfaces during an extension or flexion of the artificial joint.

Abstract: A prosthesis is provided for implantation into a body joint, such as a knee joint compartment between a femoral condyle and its corresponding tibial plateau, without requiring bone resection. The prosthesis includes a body having a generally elliptical shape in plan and including opposed top and bottom surfaces. The body includes a supporting portion and a coating portion, where the supporting portion has at least one surface at least partially disposed within an interior of the body and the coating portion has at least one surface disposed on an exterior of the body. The supporting portion is constructed from a higher modulus material than the coating portion such that the body is at least slightly deformable.

Abstract: The invention presents a total knee arthroplasty endoprosthesis having: a) a femoral component with a lower-radius lateral condyle, a larger-radius medial condyle and between them, a third condyle located posteriorly, superiorly and nearest the medial side, b) a tibial component with a central protruding spigot for the rotating polyethylene insert, and c) a rotating polyethylene insert, with three cavities for articulation of the femoral condyles. For initial and moderate flexion the joint functions with load bearing onto the lateral and medial articular cavities, and in advanced and final flexion with load bearing on the third articular cavity. The advantages of this endoprosthesis are enhanced maximum flexion, improved femoral axis alignment, significant posterior stabilization, favourable accommodation of tibial rotation with consequent relief of materials and fixations, and preservation of more articular fluid for lubrication and reduction of polyethylene wear.

Abstract: The invention relates to an artificial meniscus part for a knee-joint prosthesis that has on an upper side at least one femoral joint surface for the movable mounting of an artificial, natural or machined condyle of a femur, wherein the at least one femoral joint surface is configured in the form of a depression facing away from the meniscus part wherein the depression has an anterior and a posterior end region and a width of the depression has a minimum between the anterior and the posterior end region. An improved meniscus part set, an improved knee-joint prosthesis and an improved knee-joint prosthesis set are further proposed.

Abstract: A tibial tray assembly includes a platform having a stem extending downwardly from a bottom surface and a stem extension couple to the an end of the stem. The stem extension is electrically insulated from the stem. The tibial tray assembly also includes a wireless communication device configured to transmit data using the stem extension as an antenna.

Abstract: A prosthetic implant for securing to bone to form an articulating joint is provided. The implant is prepared by a process which includes the steps of preparing a porous surface on a component to form a prosthetic implant, placing the prosthetic implant including the porous surface in a fixture closely conforming to the porous surface of the implant and having an inlet and an opposed outlet, and directing a biological compound including stem cells into the inlet, through the porous surface of the implant and out of the outlet to form a prosthetic implant having a porous surface coated with a portion of the biological compound.

Abstract: A telemetric tibial tray includes a lower plate that defines a plurality of cylindrical transducer cavities having circular load diaphragms. An upper plate is attached to the lower plate through support posts projecting from the load diaphragms. The support posts have a circular cross-section and a diameter of about 5.0 mm. The lower plate further defines wiring channels communicating between the transducer cavities and a central cavity housing the circuit board for the telemetric tray. The wiring channels are arranged at a 45 degree angle relative to the sagittal plane of the knee joint in order to reduce the effects of the wiring channel intersection on the strain sensitivity of the tray. Each transducer cavity includes a radial strain gage array with four pairs of radially aligned strain gages, each pair aligned at a 45 degree angle relative to the sagittal plane of the knee joint.

Abstract: A knee joint prosthesis including a femoral component for attachment to a femur. The femoral component includes an anterior portion, first and second condylar portions extending from the anterior portion and having first and second bearing surfaces, the first and second condylar portions having first and second posterior ends, and a third condylar portion defined between the first and second condylar portions and extending anteriorly beyond the first and second posterior ends.

Abstract: A tibial cement impaction system and method are characterized by disposable frame and plunger elements which are used to drive bone cement under pressure into apertures formed in the top surface of the tibia to prevent a subsequently applied tibia plate or component of a knee prosthesis from loosening from the tibia. To prepare the tibia, the surgeon removes the top damaged surface of the tibia to define a relatively flat surface and drills a plurality of small holes or apertures into the surface. The holes are spaced across the surface. Next, the surgeon arranges the frame over the prepared tibia surface. The frame includes a wall having a generally kidney-shaped configuration which matches the outer perimeter of the top portion of the tibia and defines a chamber. Bone cement is arranged in the chamber and then the plunger, which is configured to match the contour of the wall, is pressed into the chamber, forcing the bone cement into the apertures and evenly across the top surface of the tibia.

Abstract: A method of performing knee-joint surgery includes positioning the tibia and the femur such that the knee-joint is disposed in a bent position. An incision is made to expose the knee-joint. A retractor support is mounted to a surgical table. The skin and flesh layers proximate the knee-joint are retracted utilizing a retractor that is attached to the retractor support which is mounted to a surgical table.

Abstract: The invention relates to a prosthetic joint which can be used as an artificial knee. Said prosthetic joint consists of a knee upper part (1), a knee lower part (2) and a fixing element (8) connecting said two lower parts. The knee upper part is rotationally arranged about the rotational axis (4) of the fixing element and rotation occurs counter to the force of an elastic element (17) which is arranged in knee lower part. Detachable fixing means (7), which are used to fix at least one rotational position, are provided between the knee upper part and the fixing element.

Abstract: A system and method for sharing and absorbing energy between body parts. In one aspect, the method involves identifying link pivot locations, fixing base components and minimally invasive insertion techniques. In one particular aspect, the system facilitates absorbing energy between members forming a joint such as between articulating bones.

Abstract: A device and a method for establishing a position and orientation for a preliminary saw cut in a distal end of a femur to prepare the femur for installation of a prosthetic knee joint. A guide block defining a cutting plane is carried on an adjustably positioned locating arm that is supported on an alignment body that can be mounted on a femur either with or without an intramedullary rod in place in the distal end of the femur. Adjustment screws and horizontal slots in the alignment body provide for varus/valgus angular adjustment of the position of the alignment body. An adjustment guide block may have a saw guiding face defining a differently oriented cutting plane.

Abstract: A system for manipulating energy transferred by members defining a joint. The system includes a first attachment structure configured to be attached to a first member of the joint and a second attachment structure configured to be attached to a second member of the joint. There is also an adjustable energy absorbing device attached to the first attachment structure and second attachment structure, wherein adjusting the energy absorbing device changes the load manipulating characteristics of the energy absorbing device.

Abstract: A joint device is disclosed for use as a prosthesis in a human or animal body. The joint device comprises a T-shaped member having a transverse pin fixedly connected to a column member and a pair of transverse sleeves configured to receive the pin and allow the pin to rotate about its longitudinal axis within the sleeves. The sleeves engage a bore in a first bone and the column member is coupled to a second bone so that the first and second bones are pivotably interconnected by the joint device. The sleeves are compressible so as to allow multi-directional movement of the bones in the joint.

Abstract: An orthopedic implant device and method is disclosed. Specifically, a knee mold system is disclosed, including elastic tibial and femoral molds, each of which may be configured and dimensioned as a unitary mold for in situ placement during a surgical procedure. Each mold may be manufactured from an elastic material that may be disposable. The tibial mold may further comprise a sidewall forming a cavity, markings for relative depth measurement, and depth rings for use as a guide for scoring, cutting, and/or trimming and tearing away an excess portion of the tibial mold. The femoral mold may further comprise a sidewall defining a cavity, two legs extending from a body of the femoral mold for forming the artificial condyles, and an eyelet for aiding in placement and removal of the femoral mold. The resulting prosthetic tibial and femoral components may form an articulation surface that mimics, at least in part, the natural articulation surface of the knee.