US20040054416A1 - Posterior stabilized knee with varus-valgus constraint - Google Patents

Posterior stabilized knee with varus-valgus constraint Download PDF

Info

Publication number
US20040054416A1
US20040054416A1 US10/242,122 US24212202A US2004054416A1 US 20040054416 A1 US20040054416 A1 US 20040054416A1 US 24212202 A US24212202 A US 24212202A US 2004054416 A1 US2004054416 A1 US 2004054416A1
Authority
US
United States
Prior art keywords
posterior
cam
spine
bearing
anterior
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/242,122
Inventor
Joe Wyss
Terry Dietz
Marc Vosler
Don Running
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DePuy Products Inc
Original Assignee
DePuy Products Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by DePuy Products Inc filed Critical DePuy Products Inc
Priority to US10/242,122 priority Critical patent/US20040054416A1/en
Assigned to DEPUY PRODUCTS, INC. reassignment DEPUY PRODUCTS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: RUNNING, DON, WYSS, JOE, DIETZ, TERRY, VOSLER, MARC C.
Priority to DK03255592T priority patent/DK1400220T3/en
Priority to ES03255592T priority patent/ES2263923T3/en
Priority to AU2003244616A priority patent/AU2003244616B2/en
Priority to AT03255592T priority patent/ATE325587T1/en
Priority to EP03255592A priority patent/EP1400220B1/en
Priority to DE60305115T priority patent/DE60305115T2/en
Publication of US20040054416A1 publication Critical patent/US20040054416A1/en
Priority to US11/121,408 priority patent/US8382847B2/en
Priority to US13/763,305 priority patent/US20130150976A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/38Joints for elbows or knees
    • A61F2/3836Special connection between upper and lower leg, e.g. constrained
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/38Joints for elbows or knees
    • A61F2/3868Joints for elbows or knees with sliding tibial bearing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/38Joints for elbows or knees
    • A61F2/3886Joints for elbows or knees for stabilising knees against anterior or lateral dislocations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30332Conically- or frustoconically-shaped protrusion and recess
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30362Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit with possibility of relative movement between the protrusion and the recess
    • A61F2002/30364Rotation about the common longitudinal axis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30383Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by laterally inserting a protrusion, e.g. a rib into a complementarily-shaped groove
    • A61F2002/3039Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by laterally inserting a protrusion, e.g. a rib into a complementarily-shaped groove with possibility of relative movement of the rib within the groove
    • A61F2002/30398Sliding
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30535Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30604Special structural features of bone or joint prostheses not otherwise provided for modular
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2220/0033Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit

Definitions

  • the present invention relates to a knee prosthesis and more particularly to a mobile bearing knee providing posterior stabilization of the anterior-posterior translation of the femoral component relative to the tibial component.
  • Flexion and extension of the normal human knee involves complex movements of the femur, the tibia and the patella.
  • flexion i.e., when the knee is bent
  • the distal end of the femur and the proximal end of the tibia roll and glide relative to each other, with the center of rotation of the joint moving posteriorly over the condyles of the femur.
  • This complex movement is typically referred to as rollback.
  • extension i.e., when the leg is straightened
  • the tibia and femur follow a reverse path. Simultaneous with the movements of the tibia and femur, the patella moves over the surface of the femoral condyles, while remaining a constant distance from the tubercle of the tibia.
  • the tibial component includes an upward projecting spine that translates within an intercondylar notch formed in the femoral component.
  • the spine can contact cam surfaces at the anterior and posterior ends of the notch to limit the relative anterior-posterior movement between the two bones.
  • the spine also operates to provide varus-valgus stability of the joint and to resist dislocation or subluxation at high angles of flexion.
  • An exemplary mobile bearing knee is disclosed in U.S. Pat. No. 6,443,991, the disclosure of which is incorporated herein by reference.
  • Other exemplary mobile bearing knees are embodied in the LCSTM System and the PFC Sigma RPTM knee system marketed by Depuy Orthopaedics, Inc., of Warsaw, Ind.
  • the present invention contemplates an improved knee prosthesis comprising a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween.
  • the notch defines an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the cam housing.
  • the prosthesis further includes a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on the platform.
  • the bearing defines medial and lateral bearing surfaces configured to articulate with the medial and lateral condyle surfaces, and a spine projecting superiorly from the bearing within the cam housing when the condyle surfaces are in articulating contact with the bearing surfaces.
  • the spine defines an anterior face facing the anterior cam and a posterior face facing the posterior cam.
  • the posterior face and the posterior cam defining complementary curved surfaces configured for cooperative engagement when the femoral component and the tibial component are rotated relative to each other to at least a predetermined flexion angle. In certain embodiments, that predetermined angle corresponds to about 50° of flexion of the knee joint.
  • the complementary curved surfaces of the posterior cam and posterior face of the spine are preferably curved at a common radius, while the anterior cam and the anterior face of the spine are substantially flat.
  • the cam housing defines a width sufficient to provide a predetermined clearance on either side of the spine, when the spine projects into the cam housing, to limit varus-valgus movement or pivoting of the joint.
  • the widths of the spine and cam housing are sized to limit varus-valgus pivoting to 0.5°-1.5°.
  • the cam housing can be configured so that a gap exists between the posterior cam and the spine when the knee is in its normally extended position.
  • the spine does not contact the posterior cam until the knee is flexed to the predetermined angle.
  • the complementary surfaces of the spine and posterior cam do not nest or coincide until the knee is flexed further to another predetermined angle.
  • the posterior cam can include a blunt or rounded anterior end that contacts the spine first when the knee is flexed. The spine and posterior cam produce roll-back for the knee prosthesis.
  • the spine has a greater height than prior spine designs.
  • the spine height is calibrated to prevent subluxation of the joint at high flexion angles.
  • the spine height is about 24.6 mm.
  • the cam housing includes a roof that is sized relative to the condyle surfaces so that the spine cannot contact the roof when the condyle surfaces are supported on the bearing surfaces.
  • the invention also contemplates a knee prosthesis comprising a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, the notch defining an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the cam housing.
  • the prosthesis also comprises a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on the platform, the bearing defining medial and lateral bearing surfaces configured to articulate with the medial and lateral condyle surfaces, and a spine projecting superiorly within the cam housing when the condyle surfaces are in articulating contact with the bearing surfaces, wherein the spine defines an anterior face facing the anterior cam and a posterior face facing the posterior cam and configured for cooperative engagement when the posterior cam.
  • the spine further defines a bore therethrough that receives a pin configured to be disposed within the bore.
  • the pin is formed of a material different from the material of the spine to add stiffness or bending strength to the spine.
  • the pin can be configured to be press-fit into the bore.
  • the spine is formed of a plastic and the pin is formed of a metal.
  • a knee prosthesis comprises a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, the notch defining an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the cam housing.
  • a tibial component includes a platform configured for attachment to the proximal end of a tibia and a bearing supported on the platform, the bearing defining medial and lateral bearing surfaces configured for rotating contact with the medial and lateral condyle surfaces.
  • a spine projects superiorly from the bearing within the cam housing when the condyle surfaces are in articulating contact with the bearing surfaces, the spine defining an anterior face facing the anterior cam and a posterior face adapted for articulating contact with the posterior cam.
  • the cam housing is configured to define an anterior-posterior distance between the anterior cam and the posterior face of the spine when the femoral component and the tibial component are in a normally extended position relative to each other.
  • the posterior face of the spine is in articulating contact with the posterior cam only at a first predetermined flexion rotation angle between the femoral component and the tibial component.
  • the first predetermined flexion angle is about 50°.
  • the posterior cam and the posterior face define complementary curved surfaces, whereby the complementary surfaces articulate relative to each other at flexion angles between the femoral component and the tibial component greater than the first predetermined flexion angle.
  • the posterior cam can include a rounded anterior end that is arranged to contact the posterior face first at the first predetermined flexion angle.
  • the complementary curved surface of the posterior cam can further be arranged on the posterior cam so that complementary curved surface of the posterior cam is substantially nested within the complementary curved surface of the posterior face of the spine only after the femoral component and the tibial component rotate relative to each other to a second predetermined flexion angle greater than the first predetermined flexion angle.
  • a more specific object is to accomplish these functions with a posterior stabilized knee that can create proper joint roll-back.
  • FIG. 1 is an exploded side view of a mobile bearing knee system according to one embodiment of the present invention.
  • FIG. 2 is an anterior view of the knee system shown in FIG. 1.
  • FIG. 3 is a lateral view of the knee system shown in FIGS. 1 and 2.
  • FIGS. 4 a - 4 c are cross-sectional view of the knee system shown in FIG. 2, taken along line 4 - 4 , with the knee system shown in its hyper-extended, normally extended, and flexed configurations.
  • FIG. 4 c includes a partial cut-away of the spine on the bearing.
  • FIG. 5 is an enlarged diagram illustrating roll-back of the contact point between the femoral and tibial components of the mobile bearing knee system shown in FIG. 4 c.
  • a knee system 10 that includes a femoral component 12 and a tibial component 14 .
  • the tibial component includes a tibial platform 16 from which extends a tibial stem 18 that is configured for engagement within the prepared end of the tibia.
  • a bearing 20 is rotatably mounted on the platform 16 by way of a bearing stem 22 that fits within a complementary socket 24 within the platform.
  • the bearing 20 defines an upper bearing surface that supports the femoral component. More specifically, the bearing 20 includes a lateral bearing surface 26 and a medial bearing surface 28 . These bearing surfaces 26 , 28 are configured for articulating support of corresponding condyle bearings 30 , 32 of the femoral component 12 . This articulating or sliding support is best seen in FIGS. 2 and 3.
  • the femoral component 12 is configured to emulate the configuration of the femoral condyles.
  • the component 12 includes an anterior portion 34 and a posterior portion 36 that are curved in the manner of the natural condyles.
  • the anterior portion 34 defines a patellar groove 49 that is configured to orient a patellar implant (not shown) in a manner known in the art.
  • the femoral component 12 utilizes a number of surfaces to fix the component to the prepared end of the femur.
  • the inner surface 37 of the anterior and posterior portions 34 , 36 are configured to directly interface over the prepared end of the femur.
  • a stem 38 can be provided that is fixed within the femur.
  • the femoral component 12 can include an intercondylar notch 40 formed by a pair of opposite side walls 44 and a roof 46 .
  • the prosthetic knee 10 can assume a variety of known configurations.
  • the femoral component 12 and tibial component 14 as described above can have the configuration of like components of the mobile bearing knee described in U.S. Pat. No. 6,443,991, the description of which is incorporated by reference.
  • the knee 10 of the present invention includes a spine 60 that projects from the upper surface 25 of the bearing 20 .
  • the spine 60 resides within a cam housing 42 (FIG. 3) that is essentially formed by the walls of the intercondylar notch 40 .
  • the spine 60 is sized relative to the cam housing 42 to provide a measured degree of varus-valgus constraint.
  • the spine 60 has a width W 1 that is slightly less than the width W 2 of the cam housing 42 at the intercondylar notch 40 (FIG. 1).
  • width W 1 is sized relative to the width W 2 to provide 0.13 mm clearance on each side of the spine.
  • this clearance should be limited to from about 0.12 mm to about 0.50 mm per side to avoid excessive varus-valgus movement of the knee components 12 , 14 relative to each other.
  • this clearance permits about 1.25° of varus-valgus pivoting.
  • each of the components must be sized to the skeletal dimensions of the patient.
  • the femoral component 12 and tibial component 14 can be provided in several sizes, and preferably in six sizes ranging from small to extra-large.
  • the tibial spine 60 can have a width W 1 of about 17.5 mm.
  • the cam housing 42 would have a width W 2 of 17.76 mm to provide the proper side-to-side clearance for the spine 60 .
  • the dimensions of the spine and the cam housing can be appropriately proportioned for other sizes of knee components.
  • the spine 60 interacts with the cam housing 42 to prevent subluxation of the knee 10 .
  • the spine 60 defines a subluxation height from the bearing surface 25 that corresponds to the distance that the femoral component must be raised relative to the tibial component until the femoral component is clear of the top of the spine.
  • Subluxation is generally not a problem when the knee is straightened (as shown in FIGS. 3 and 4 b ), but can be problematic when the knee is flexed (as shown in FIG. 4 c ).
  • the subluxation height is measured at a certain degree of flexion, most typically at 120° of flexion. (For comparison, the knee in FIG. 4 c is shown at approximately 80° of flexion).
  • the spine has an effective height of between 16-24 mm, and most preferably 19.3 mm, when the prosthesis is at 90° flexion.
  • the femoral component must rise off the tibial bearing 20 by at least 19.3 mm to cause a dislocation of the knee.
  • the natural ligaments and surrounding soft tissues of the knee provide sufficient resistance to femoral lift-off greater than this subluxation height, especially at high flexion angles.
  • the cam housing 42 defines an anterior cam 50 having a cam face 51 .
  • This anterior cam 50 is adjacent the anterior portion 34 of the tibial component 12 .
  • the cam face 51 is substantially flat.
  • the spine 60 has an anterior face 62 that is also substantially flat. The cam face 51 and anterior face 62 are arranged to restrict extension of the knee in the anterior direction (as designated by the arrow A in FIG. 4 a ).
  • the spine 60 can contact the anterior cam 50 to prevent further movement in the anterior direction.
  • this contact can occur at about 5° hyperextension.
  • tension in the ligaments supporting and surrounding the knee will prevent hyper-extension of the knee, and ideally will prevent contact between the spine and the anterior cam 50 .
  • the cam housing further defines a posterior cam 55 at the opposite end of the intercondylar notch 40 from the anterior cam 50 , as shown in FIG. 3.
  • the posterior cam 55 defines a curved surface 56 that cooperates with a curved posterior face 64 of the spine, as best shown in FIG. 4 c.
  • These cooperating surfaces are configured for optimum roll-back characteristics of the prosthetic knee 10 .
  • the contact point between the tibial and femoral components, as well as the axis of rotation of the tibia relative to the femur to shift posteriorly (as designated by the direction arrow P in FIG. 4 a ). This posterior shift optimizes the moment arm and reduces the strain on the quadricep muscle responsible for flexing the knee.
  • the cam housing 42 is elongated between the anterior and posterior cams so that the bearing 20 , and particularly the spine 60 , can articulate as the knee is initially flexed and the condyle bearings 30 , 32 rotate on the bearing surfaces 26 , 28 .
  • the posterior face 64 of the spine 60 contacts the posterior cam 55 .
  • This contact between spine and cam provides posterior stability to the knee 10 as the knee continues to flex.
  • the mating surfaces are complementary curved, as best illustrated in FIGS. 4 a - 4 b.
  • the posterior face 64 of the spine 60 is concave from the bearing surface 25 of the bearing 20 to the posterior peak 66 at the top of the spine.
  • the posteriorly directed peak 66 provides additional posterior stability and resistance to subluxation at high flexion angles of 120° and beyond.
  • the curvature or concavity of the posterior face 64 is selected to permit a predetermined amount of roll-back, while maintaining the posterior stability afforded by the spine-to-cam contact.
  • This roll-back is depicted in FIG. 5.
  • the contact point designated C 1 corresponds to the initial contact between the spine and the posterior cam.
  • the contact point shifts posteriorly to the contact point C 2 .
  • the posterior face 64 is configured to permit roll-back of between 0.0 mm up to about 5.0 mm. Most preferably this roll-back is about 4.2 mm.
  • the curved posterior face 64 of the spine 60 is concave at a radius of between 28-32 mm. Most preferably, the radius of the posterior face is about 30 mm.
  • the curved posterior face 64 transitions into the posterior peak 66 , which is preferably rounded. In a preferred embodiment, this peak is formed at a radius of about 5 mm. Since the curved surface 55 of the posterior cam is complementary to the posterior face 64 , it too has a most preferred radius of 30 mm.
  • At least the anterior end 57 of the posterior cam 55 is blunted or rounded to provide a smooth transition when the cam contacts the spine 60 .
  • the opposite posterior end of the cam 55 can also be rounded, as shown in the figures. This rounded anterior end 57 is the first portion of the posterior cam to contact the spine as the knee is flexed to the predetermined flexion angle. Nominally, the anterior end 57 will initially contact the spine 60 below the rounded posterior peak 66 .
  • the curved posterior face 64 of the spine is curved along substantially the entire height of the spine 60 .
  • the posterior cam 55 or more particularly the curved surface 56 of the cam, has a length that is substantially equal to the length or height of the curved face of the spine.
  • the curved surface of the posterior cam is completely nested within the concave posterior face of the spine.
  • This complementary interface can then operate as a fulcrum or pivot point for further relative rotation between the tibial and femoral components. While the condyle bearings and bearing surfaces continue to articulate relative to each other, the greater share of the shear load can now be borne by the complementary interface between the posterior cam 55 and the posterior face 64 of the spine 60 .
  • This interface can thus preserve the mechanical advantage of the quadricep muscle through high flexion angles.
  • the kinematics of this spine/cam interface allows a patellar implant to easily follow the patellar track 49 without placing undue stress on the patellar tendons.
  • the spine 60 has an anterior-posterior dimension that is significantly less than the distance between the anterior and posterior cams 50 , 55 in the cam housing 42 . From the limit of extension, shown in FIG. 4 a, to the normal straight leg position of FIG. 4 b the spine does not contact the cam housing and therefore does not either bear any knee loads or dictate any knee motion.
  • the cam housing 42 is elongated with a distance between anterior and posterior cams that is significantly greater than the anterior-posterior (a-p) dimension of the spine.
  • the distance between cams is about 1.5 times the a-p dimension of the spine.
  • the a-p dimension of the spine is about 10.0 mm at the posterior peak 66
  • the distance between the anterior cam face 51 and the anterior end of the posterior cam 55 is about 15.0 mm.
  • the knee load is carried solely by the articulating interface between the condyle bearings 30 , 32 and the bearing surfaces 26 , 28 .
  • the quadricep muscles enjoy their greatest moment arm and mechanical advantage.
  • the femoral component 12 moves posteriorly relative to the tibial component 14 so the quadricep mechanical advantage gradually decreases.
  • the present invention contemplates that the posterior face 64 of the spine will contact the posterior cam 55 after a pre-determined amount of flexion. In a preferred embodiment, this pre-determined amount of flexion of about 50°.
  • the spine and posterior cam cooperate to provide an additional articulating bearing interface to not only share in the shear loads, but also to provide a fulcrum or reaction surface working against the quadricep muscle to preserve the flexion moment arm and mechanical advantage.
  • the posterior cam 55 becomes fully seated within the concave posterior face 64 of the spine to maximize the bearing contact between these two components.
  • the stem 22 of the bearing 20 defines a central bore 70 at least partially therethrough, as shown in FIG. 4 b.
  • a stiffening pin 72 can be pressed into the bore 70 , as shown in FIG. 4 c.
  • the pin 72 can be formed of a stiff metal, such as a cobalt chrome alloy.
  • the prosthetic components designed to engage the natural bone are formed of a biocompatible metal, such as cobalt chrome alloy.
  • the bone engaging surfaces of these components can be textured to facilitate cementing the component to the bone, or can be porous coated to promote bone ingrowth for permanent fixation.
  • the bearing 20 is most preferably formed of a material that allows for smooth articulation and rotation between the bearing and the other components.
  • the material is selected to meet several criteria, such as producing as little friction as possible between the articulating/rotating surfaces, providing as much wear resistance as possible, and remaining as strong as possible.
  • One preferred material is ultra-high molecular weight polyethylene (UHMWPe) because it optimizes these three and other criteria.
  • the spine 60 must bear significant loads in the transverse and coronal planes—i.e., lateral to the spine axis.
  • the spine 60 can be provided as a separate component that mates with the remainder of the bearing 20 .
  • the spine can be formed of a high strength metal, such as the cobalt alloy mentioned above. This approach adds to the complexity of the knee construct and adds the problem of interfacing the spine to the remainder of the bearing.
  • the spine 60 be integrally formed with the bearing 20 , which means that the spine will be formed of the same material. Where this material is UHMWPe, transverse or shear strength, and even bending stiffness, becomes a design consideration, particularly for active patients.
  • the stiffening pin 72 can extend through the axis of the spine 60 to add bending stiffness and shear resistance to the spine.
  • the pin 72 can be provided in different lengths depending upon the desired effect.
  • the pin can be sized for insertion from the top of the spine 60 and to only extend for the height of the spine.
  • the pin can be introduced from the bottom of the bearing stem 22 and can include a stepped diameter to be press-fit into a comparable stepped diameter bore 70 of the stem 22 .
  • the preferred embodiment contemplates one form of mobile bearing knee in which the tibial bearing rotates relative to the tibial platform.
  • Other mobile bearing knees are contemplated, including knee prostheses in which the bearing slides on the platform.
  • the inventive concepts can also be implemented in knee prosthesis in which the bearing does not move or is incorporated into the tibial platform.
  • the illustrated embodiments contemplate that the spine projects from the bearing.
  • the inventive concepts can be implemented where the spine is separate from the bearing, whether as a separate insert or integrated with the tibial platform.

Abstract

A femoral component of a knee prosthesis has spaced condyle surfaces defining a notch therebetween. The notch defines an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the housing. The tibial component of the knee prosthesis includes a platform and a bearing supported on the platform, the bearing defining bearing surfaces configured to articulate with the condyle surfaces. The tibial component includes a spine projecting superiorly from the bearing that defines an anterior face and a posterior face. The posterior face and the posterior cam define complementary curved surfaces configured for cooperative engagement when the femoral component and the tibial component are at a predetermined flexion angle. The cam housing is configured to form a gap between the posterior cam and the spine when the knee is normally extended. In another feature, the spine includes a stiffening pin extending therethrough.

Description

    BACKGROUND OF THE INVENTION
  • The present invention relates to a knee prosthesis and more particularly to a mobile bearing knee providing posterior stabilization of the anterior-posterior translation of the femoral component relative to the tibial component. [0001]
  • Flexion and extension of the normal human knee involves complex movements of the femur, the tibia and the patella. During flexion (i.e., when the knee is bent), the distal end of the femur and the proximal end of the tibia roll and glide relative to each other, with the center of rotation of the joint moving posteriorly over the condyles of the femur. This complex movement is typically referred to as rollback. During extension (i.e., when the leg is straightened), the tibia and femur follow a reverse path. Simultaneous with the movements of the tibia and femur, the patella moves over the surface of the femoral condyles, while remaining a constant distance from the tubercle of the tibia. [0002]
  • Damage or disease can deteriorate the bones, articular cartilage and ligaments of the knee, which can ultimately affect the ability of the natural knee to function properly. To address these conditions, prosthetic knees have been developed that are mounted to prepared ends of the femur and tibia. Among the many knee prostheses, a mobile bearing knee simulates the condylar and bearing surfaces of the knee to emulate the natural movement of the knee during flexion and extension. The tibial component is configured to permit rotation about the axis of the tibia to accurately replicate the effects of differential rollback in the transverse plane. [0003]
  • In one type of mobile bearing knee, the tibial component includes an upward projecting spine that translates within an intercondylar notch formed in the femoral component. The spine can contact cam surfaces at the anterior and posterior ends of the notch to limit the relative anterior-posterior movement between the two bones. The spine also operates to provide varus-valgus stability of the joint and to resist dislocation or subluxation at high angles of flexion. An exemplary mobile bearing knee is disclosed in U.S. Pat. No. 6,443,991, the disclosure of which is incorporated herein by reference. Other exemplary mobile bearing knees are embodied in the LCS™ System and the PFC Sigma RP™ knee system marketed by Depuy Orthopaedics, Inc., of Warsaw, Ind. [0004]
  • While mobile bearing knees are thought to most accurately mimic the natural movement of the intact knee, the design of knee systems requires the introduction of features to maintain the stability of the artificial joint. Thus, modern knee systems provide additional stability to posterior stabilized devices to prevent hyperextension. The articulating and rotating components of the knee system must do so smoothly and accurately. At the same time, the natural knee permits a certain amount of movement and pivoting in the transverse and coronal planes that should be approximated in the prosthetic knee system. The development of knee systems has attempted to harmonize the need for preserving a full range of motion with the need for maintaining the strength of the joint. [0005]
  • SUMMARY OF THE INVENTION
  • The present invention contemplates an improved knee prosthesis comprising a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween. The notch defines an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the cam housing. [0006]
  • The prosthesis further includes a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on the platform. The bearing defines medial and lateral bearing surfaces configured to articulate with the medial and lateral condyle surfaces, and a spine projecting superiorly from the bearing within the cam housing when the condyle surfaces are in articulating contact with the bearing surfaces. [0007]
  • The spine defines an anterior face facing the anterior cam and a posterior face facing the posterior cam. In one feature of the invention, the posterior face and the posterior cam defining complementary curved surfaces configured for cooperative engagement when the femoral component and the tibial component are rotated relative to each other to at least a predetermined flexion angle. In certain embodiments, that predetermined angle corresponds to about 50° of flexion of the knee joint. [0008]
  • The complementary curved surfaces of the posterior cam and posterior face of the spine are preferably curved at a common radius, while the anterior cam and the anterior face of the spine are substantially flat. [0009]
  • In one aspect of the knee prosthesis the cam housing defines a width sufficient to provide a predetermined clearance on either side of the spine, when the spine projects into the cam housing, to limit varus-valgus movement or pivoting of the joint. In a preferred embodiment, the widths of the spine and cam housing are sized to limit varus-valgus pivoting to 0.5°-1.5°. [0010]
  • In addition, the cam housing can be configured so that a gap exists between the posterior cam and the spine when the knee is in its normally extended position. The spine does not contact the posterior cam until the knee is flexed to the predetermined angle. In another aspect, the complementary surfaces of the spine and posterior cam do not nest or coincide until the knee is flexed further to another predetermined angle. The posterior cam can include a blunt or rounded anterior end that contacts the spine first when the knee is flexed. The spine and posterior cam produce roll-back for the knee prosthesis. [0011]
  • In yet another aspect of the invention, the spine has a greater height than prior spine designs. The spine height is calibrated to prevent subluxation of the joint at high flexion angles. In a preferred embodiment, the spine height is about 24.6 mm. The cam housing includes a roof that is sized relative to the condyle surfaces so that the spine cannot contact the roof when the condyle surfaces are supported on the bearing surfaces. [0012]
  • The invention also contemplates a knee prosthesis comprising a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, the notch defining an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the cam housing. The prosthesis also comprises a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on the platform, the bearing defining medial and lateral bearing surfaces configured to articulate with the medial and lateral condyle surfaces, and a spine projecting superiorly within the cam housing when the condyle surfaces are in articulating contact with the bearing surfaces, wherein the spine defines an anterior face facing the anterior cam and a posterior face facing the posterior cam and configured for cooperative engagement when the posterior cam. [0013]
  • In this embodiment, the spine further defines a bore therethrough that receives a pin configured to be disposed within the bore. The pin is formed of a material different from the material of the spine to add stiffness or bending strength to the spine. The pin can be configured to be press-fit into the bore. In certain embodiments, the spine is formed of a plastic and the pin is formed of a metal. [0014]
  • In still another aspect of the invention, a knee prosthesis comprises a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, the notch defining an elongated cam housing having an anterior cam and a posterior cam at opposite ends of the cam housing. A tibial component includes a platform configured for attachment to the proximal end of a tibia and a bearing supported on the platform, the bearing defining medial and lateral bearing surfaces configured for rotating contact with the medial and lateral condyle surfaces. A spine projects superiorly from the bearing within the cam housing when the condyle surfaces are in articulating contact with the bearing surfaces, the spine defining an anterior face facing the anterior cam and a posterior face adapted for articulating contact with the posterior cam. [0015]
  • With this embodiment, the cam housing is configured to define an anterior-posterior distance between the anterior cam and the posterior face of the spine when the femoral component and the tibial component are in a normally extended position relative to each other. With this configuration, the posterior face of the spine is in articulating contact with the posterior cam only at a first predetermined flexion rotation angle between the femoral component and the tibial component. In a specific embodiment, the first predetermined flexion angle is about 50°. [0016]
  • This embodiment further contemplates that the posterior cam and the posterior face define complementary curved surfaces, whereby the complementary surfaces articulate relative to each other at flexion angles between the femoral component and the tibial component greater than the first predetermined flexion angle. The posterior cam can include a rounded anterior end that is arranged to contact the posterior face first at the first predetermined flexion angle. The complementary curved surface of the posterior cam can further be arranged on the posterior cam so that complementary curved surface of the posterior cam is substantially nested within the complementary curved surface of the posterior face of the spine only after the femoral component and the tibial component rotate relative to each other to a second predetermined flexion angle greater than the first predetermined flexion angle. [0017]
  • It is one object of the present invention to provide a prosthetic knee that accurately and efficiently emulates the kinematics and function of a normal, health knee. A more specific object is to accomplish these functions with a posterior stabilized knee that can create proper joint roll-back. [0018]
  • Another object is accomplished by features of the invention that restrict varus-valgus movement or pivoting, as well as provide resistance to subluxation. Other objects and certain benefits of the invention can be appreciated from the following written description together with the accompanying figures. [0019]
  • DESCRIPTION OF THE FIGURES
  • FIG. 1 is an exploded side view of a mobile bearing knee system according to one embodiment of the present invention. [0020]
  • FIG. 2 is an anterior view of the knee system shown in FIG. 1. [0021]
  • FIG. 3 is a lateral view of the knee system shown in FIGS. 1 and 2. [0022]
  • FIGS. 4[0023] a-4 c are cross-sectional view of the knee system shown in FIG. 2, taken along line 4-4, with the knee system shown in its hyper-extended, normally extended, and flexed configurations. FIG. 4c includes a partial cut-away of the spine on the bearing.
  • FIG. 5 is an enlarged diagram illustrating roll-back of the contact point between the femoral and tibial components of the mobile bearing knee system shown in FIG. 4[0024] c.
  • DESCRIPTION OF THE PREFERRED EMBODIMENT
  • For the purposes of promoting an understanding of the principles of the invention, reference will now be made to the embodiments illustrated in the drawings and described in the following written specification. It is understood that no limitation to the scope of the invention is thereby intended. It is further understood that the present invention includes any alterations and modifications to the illustrated embodiments and includes further applications of the principles of the invention as would normally occur to one skilled in the art to which this invention pertains. [0025]
  • Referring to FIG. 1, a [0026] knee system 10 is depicted that includes a femoral component 12 and a tibial component 14. The tibial component includes a tibial platform 16 from which extends a tibial stem 18 that is configured for engagement within the prepared end of the tibia. A bearing 20 is rotatably mounted on the platform 16 by way of a bearing stem 22 that fits within a complementary socket 24 within the platform.
  • The [0027] bearing 20 defines an upper bearing surface that supports the femoral component. More specifically, the bearing 20 includes a lateral bearing surface 26 and a medial bearing surface 28. These bearing surfaces 26, 28 are configured for articulating support of corresponding condyle bearings 30, 32 of the femoral component 12. This articulating or sliding support is best seen in FIGS. 2 and 3.
  • The [0028] femoral component 12 is configured to emulate the configuration of the femoral condyles. Thus, the component 12 includes an anterior portion 34 and a posterior portion 36 that are curved in the manner of the natural condyles. The anterior portion 34 defines a patellar groove 49 that is configured to orient a patellar implant (not shown) in a manner known in the art.
  • The [0029] femoral component 12 utilizes a number of surfaces to fix the component to the prepared end of the femur. The inner surface 37 of the anterior and posterior portions 34, 36, are configured to directly interface over the prepared end of the femur. In addition, a stem 38 can be provided that is fixed within the femur. In addition, the femoral component 12 can include an intercondylar notch 40 formed by a pair of opposite side walls 44 and a roof 46.
  • As thus far described, the [0030] prosthetic knee 10 can assume a variety of known configurations. For instance, the femoral component 12 and tibial component 14 as described above can have the configuration of like components of the mobile bearing knee described in U.S. Pat. No. 6,443,991, the description of which is incorporated by reference.
  • As with the prior mobile bearing knee of the '991 Patent, the [0031] knee 10 of the present invention includes a spine 60 that projects from the upper surface 25 of the bearing 20. The spine 60 resides within a cam housing 42 (FIG. 3) that is essentially formed by the walls of the intercondylar notch 40. In one aspect of the present invention, the spine 60 is sized relative to the cam housing 42 to provide a measured degree of varus-valgus constraint. The spine 60 has a width W1 that is slightly less than the width W2 of the cam housing 42 at the intercondylar notch 40 (FIG. 1). These two widths are sized relative to each other to limit varus-valgus movement or pivoting to a range of about 0.5°-2.5°. In a specific preferred embodiment of the invention, the width W1 is sized relative to the width W2 to provide 0.13 mm clearance on each side of the spine. Preferably, this clearance should be limited to from about 0.12 mm to about 0.50 mm per side to avoid excessive varus-valgus movement of the knee components 12, 14 relative to each other. In the specific embodiment, this clearance permits about 1.25° of varus-valgus pivoting.
  • As with other known prosthetic knees, each of the components must be sized to the skeletal dimensions of the patient. Thus, it is contemplated that the [0032] femoral component 12 and tibial component 14 can be provided in several sizes, and preferably in six sizes ranging from small to extra-large. For a medium sized knee, the tibial spine 60 can have a width W1 of about 17.5 mm. In accordance with the specific embodiment discussed above (i.e., with a 0.13 mm clearance on each side), the cam housing 42 would have a width W2 of 17.76 mm to provide the proper side-to-side clearance for the spine 60. The dimensions of the spine and the cam housing can be appropriately proportioned for other sizes of knee components.
  • In addition to providing a measured degree of varus-valgus constraint, the [0033] spine 60 interacts with the cam housing 42 to prevent subluxation of the knee 10. In particular, the spine 60 defines a subluxation height from the bearing surface 25 that corresponds to the distance that the femoral component must be raised relative to the tibial component until the femoral component is clear of the top of the spine. Subluxation is generally not a problem when the knee is straightened (as shown in FIGS. 3 and 4b), but can be problematic when the knee is flexed (as shown in FIG. 4c). Thus, the subluxation height is measured at a certain degree of flexion, most typically at 120° of flexion. (For comparison, the knee in FIG. 4c is shown at approximately 80° of flexion).
  • In accordance with the preferred embodiment of the present invention, the spine has an effective height of between 16-24 mm, and most preferably 19.3 mm, when the prosthesis is at 90° flexion. Thus, the femoral component must rise off the [0034] tibial bearing 20 by at least 19.3 mm to cause a dislocation of the knee. The natural ligaments and surrounding soft tissues of the knee provide sufficient resistance to femoral lift-off greater than this subluxation height, especially at high flexion angles.
  • Referring now to FIGS. 3 and 4[0035] a-c, a further feature of the present invention is depicted. In particular, the cam housing 42 defines an anterior cam 50 having a cam face 51. This anterior cam 50 is adjacent the anterior portion 34 of the tibial component 12. As seen in FIGS. 3 and 4a, the cam face 51 is substantially flat. Similarly, the spine 60 has an anterior face 62 that is also substantially flat. The cam face 51 and anterior face 62 are arranged to restrict extension of the knee in the anterior direction (as designated by the arrow A in FIG. 4a). Thus, as the tibia, and hence the tibial component 14, moves anteriorly relative to the femur and femoral component 12, the spine 60 can contact the anterior cam 50 to prevent further movement in the anterior direction. In the illustrated embodiment, this contact can occur at about 5° hyperextension. However, tension in the ligaments supporting and surrounding the knee will prevent hyper-extension of the knee, and ideally will prevent contact between the spine and the anterior cam 50.
  • The cam housing further defines a [0036] posterior cam 55 at the opposite end of the intercondylar notch 40 from the anterior cam 50, as shown in FIG. 3. The posterior cam 55 defines a curved surface 56 that cooperates with a curved posterior face 64 of the spine, as best shown in FIG. 4c. These cooperating surfaces are configured for optimum roll-back characteristics of the prosthetic knee 10. As the knee is flexed from the neutral position depicted in FIG. 4b to the position shown in FIG. 4c, it is desirable for the contact point between the tibial and femoral components, as well as the axis of rotation of the tibia relative to the femur, to shift posteriorly (as designated by the direction arrow P in FIG. 4a). This posterior shift optimizes the moment arm and reduces the strain on the quadricep muscle responsible for flexing the knee.
  • As shown in FIG. 4[0037] b, the cam housing 42 is elongated between the anterior and posterior cams so that the bearing 20, and particularly the spine 60, can articulate as the knee is initially flexed and the condyle bearings 30, 32 rotate on the bearing surfaces 26, 28. As the knee continues to rotate to about 50° of flexion, the posterior face 64 of the spine 60 contacts the posterior cam 55. This contact between spine and cam provides posterior stability to the knee 10 as the knee continues to flex. In order to accommodate continued femoral roll-back, the mating surfaces are complementary curved, as best illustrated in FIGS. 4a-4 b. Specifically, the posterior face 64 of the spine 60 is concave from the bearing surface 25 of the bearing 20 to the posterior peak 66 at the top of the spine. The posteriorly directed peak 66 provides additional posterior stability and resistance to subluxation at high flexion angles of 120° and beyond.
  • The curvature or concavity of the [0038] posterior face 64 is selected to permit a predetermined amount of roll-back, while maintaining the posterior stability afforded by the spine-to-cam contact. This roll-back is depicted in FIG. 5. The contact point designated C1 corresponds to the initial contact between the spine and the posterior cam. When the knee is flexed further, the contact point shifts posteriorly to the contact point C2. In a preferred embodiment, the posterior face 64 is configured to permit roll-back of between 0.0 mm up to about 5.0 mm. Most preferably this roll-back is about 4.2 mm. Thus, as the knee continues to flex from the 50° point of contact between spine and posterior cam, the curved surface 56 of the cam nestles into the curved posterior face 64. At the same time, the contact point between the femoral component 12 and the tibial component 14 shifts posteriorly. Continued flexing causes the curved cam surface 56 to articulate within the concave posterior face 64 of the spine, which further shifts the contact point in the posterior direction.
  • In a preferred embodiment, the [0039] curved posterior face 64 of the spine 60 is concave at a radius of between 28-32 mm. Most preferably, the radius of the posterior face is about 30 mm. The curved posterior face 64 transitions into the posterior peak 66, which is preferably rounded. In a preferred embodiment, this peak is formed at a radius of about 5 mm. Since the curved surface 55 of the posterior cam is complementary to the posterior face 64, it too has a most preferred radius of 30 mm.
  • At least the [0040] anterior end 57 of the posterior cam 55 is blunted or rounded to provide a smooth transition when the cam contacts the spine 60. The opposite posterior end of the cam 55 can also be rounded, as shown in the figures. This rounded anterior end 57 is the first portion of the posterior cam to contact the spine as the knee is flexed to the predetermined flexion angle. Nominally, the anterior end 57 will initially contact the spine 60 below the rounded posterior peak 66.
  • The [0041] curved posterior face 64 of the spine is curved along substantially the entire height of the spine 60. Moreover, the posterior cam 55, or more particularly the curved surface 56 of the cam, has a length that is substantially equal to the length or height of the curved face of the spine. At about 120° of flexion, the curved surface of the posterior cam is completely nested within the concave posterior face of the spine. This complementary interface can then operate as a fulcrum or pivot point for further relative rotation between the tibial and femoral components. While the condyle bearings and bearing surfaces continue to articulate relative to each other, the greater share of the shear load can now be borne by the complementary interface between the posterior cam 55 and the posterior face 64 of the spine 60. This interface can thus preserve the mechanical advantage of the quadricep muscle through high flexion angles. In addition, the kinematics of this spine/cam interface allows a patellar implant to easily follow the patellar track 49 without placing undue stress on the patellar tendons.
  • Referring to FIG. 4[0042] b, it can be seen that the spine 60 has an anterior-posterior dimension that is significantly less than the distance between the anterior and posterior cams 50, 55 in the cam housing 42. From the limit of extension, shown in FIG. 4a, to the normal straight leg position of FIG. 4b the spine does not contact the cam housing and therefore does not either bear any knee loads or dictate any knee motion. In one feature of the invention, the cam housing 42 is elongated with a distance between anterior and posterior cams that is significantly greater than the anterior-posterior (a-p) dimension of the spine. In a preferred embodiment, the distance between cams is about 1.5 times the a-p dimension of the spine. In one specific embodiment, the a-p dimension of the spine is about 10.0 mm at the posterior peak 66, and the distance between the anterior cam face 51 and the anterior end of the posterior cam 55 is about 15.0 mm.
  • With this configuration, the knee load is carried solely by the articulating interface between the [0043] condyle bearings 30, 32 and the bearing surfaces 26, 28. As the knee starts to flex from the straightened position shown in FIG. 4b the quadricep muscles enjoy their greatest moment arm and mechanical advantage. As the knee continues to flex, the femoral component 12 moves posteriorly relative to the tibial component 14 so the quadricep mechanical advantage gradually decreases.
  • In order to preserve the quadricep mechanical advantage, the present invention contemplates that the [0044] posterior face 64 of the spine will contact the posterior cam 55 after a pre-determined amount of flexion. In a preferred embodiment, this pre-determined amount of flexion of about 50°. At this point, the spine and posterior cam cooperate to provide an additional articulating bearing interface to not only share in the shear loads, but also to provide a fulcrum or reaction surface working against the quadricep muscle to preserve the flexion moment arm and mechanical advantage. As the flexion continues, the posterior cam 55 becomes fully seated within the concave posterior face 64 of the spine to maximize the bearing contact between these two components.
  • In another aspect of the invention, the [0045] stem 22 of the bearing 20 defines a central bore 70 at least partially therethrough, as shown in FIG. 4b. A stiffening pin 72 can be pressed into the bore 70, as shown in FIG. 4c. The pin 72 can be formed of a stiff metal, such as a cobalt chrome alloy.
  • In accordance with accepted practice, the prosthetic components designed to engage the natural bone, such as the [0046] femoral component 12 and the tibial platform 16, are formed of a biocompatible metal, such as cobalt chrome alloy. The bone engaging surfaces of these components can be textured to facilitate cementing the component to the bone, or can be porous coated to promote bone ingrowth for permanent fixation.
  • However, the [0047] bearing 20 is most preferably formed of a material that allows for smooth articulation and rotation between the bearing and the other components. The material is selected to meet several criteria, such as producing as little friction as possible between the articulating/rotating surfaces, providing as much wear resistance as possible, and remaining as strong as possible. One preferred material is ultra-high molecular weight polyethylene (UHMWPe) because it optimizes these three and other criteria.
  • One concern posed by the material used for the [0048] spine 60 is that the spine must bear significant loads in the transverse and coronal planes—i.e., lateral to the spine axis. In one approach, the spine 60 can be provided as a separate component that mates with the remainder of the bearing 20. With this approach, the spine can be formed of a high strength metal, such as the cobalt alloy mentioned above. This approach adds to the complexity of the knee construct and adds the problem of interfacing the spine to the remainder of the bearing.
  • It is preferred that the [0049] spine 60 be integrally formed with the bearing 20, which means that the spine will be formed of the same material. Where this material is UHMWPe, transverse or shear strength, and even bending stiffness, becomes a design consideration, particularly for active patients. To address this concern, the stiffening pin 72 can extend through the axis of the spine 60 to add bending stiffness and shear resistance to the spine. The pin 72 can be provided in different lengths depending upon the desired effect. For instance, the pin can be sized for insertion from the top of the spine 60 and to only extend for the height of the spine. Alternatively, as shown in FIG. 4c, the pin can be introduced from the bottom of the bearing stem 22 and can include a stepped diameter to be press-fit into a comparable stepped diameter bore 70 of the stem 22.
  • While the invention has been illustrated and described in detail in the drawings and foregoing description, the same should be considered as illustrative and not restrictive in character. It is understood that only the preferred embodiments have been presented and that all changes, modifications and further applications that come within the spirit of the invention are desired to be protected. [0050]
  • For instance, the preferred embodiment contemplates one form of mobile bearing knee in which the tibial bearing rotates relative to the tibial platform. Other mobile bearing knees are contemplated, including knee prostheses in which the bearing slides on the platform. Of course, the inventive concepts can also be implemented in knee prosthesis in which the bearing does not move or is incorporated into the tibial platform. [0051]
  • In addition, the illustrated embodiments contemplate that the spine projects from the bearing. The inventive concepts can be implemented where the spine is separate from the bearing, whether as a separate insert or integrated with the tibial platform. [0052]

Claims (26)

What is claimed is:
1. A knee prosthesis comprising:
a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, said notch defining an elongated cam housing having a posterior cam at one end of said cam housing; and
a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on said platform, said bearing defining medial and lateral bearing surfaces configured to articulate with said medial and lateral condyle surfaces, and a spine projecting superiorly from said bearing within said cam housing when said condyle surfaces are in articulating contact with said bearing surfaces,
wherein said spine defines an anterior face and an opposite posterior face facing said posterior cam, said posterior face and said posterior cam defining complementary curved surfaces configured for cooperative engagement when said femoral component and said tibial component are rotated relative to each other to at least a predetermined flexion angle.
2. The knee prosthesis according to claim 1, wherein said complementary curved surface of said posterior face of said spine is concave at a radius, and said complementary curved surface of said cam is curved at substantially said radius.
3. The knee prosthesis according to claim 1, wherein:
said cam housing defines an anterior cam at an opposite end thereof; and
said anterior face of said spine facing said anterior cam is substantially flat.
4. The knee prosthesis according to claim 3, wherein said anterior cam defines a substantially flat surface complementary to said anterior face of said spine.
5. The knee prosthesis according to claim 1, wherein said cam housing defines a width sufficient to provide a clearance ranging between about 0.0 mm to about 0.13 mm on either side of said spine when said spine projects into said cam housing, whereby said spine and said cam housing interact to restrict varus-valgus pivoting between said femoral component and said tibial component.
6. The knee prosthesis according to claim 1, wherein said cam housing each define a width sized relative each other so that said spine and said cam housing interact to restrict varus-valgus pivoting between said femoral component and said tibial component to between 0.5° and 2.5°.
7. The knee prosthesis according to claim 1, wherein said spine has a height of about 16.0-24. mm and said cam housing includes a roof and is sized relative to said condyle surfaces so that said spine cannot contact said roof when said condyle surfaces are supported on said bearing surfaces.
8. The knee prosthesis according to claim 7, wherein said complementary curved surface of said posterior face of said spine is concave at a radius and has a length sized so that said curved surface extends along substantially the entire height of said spine.
9. The knee prosthesis according to claim 8, wherein said spine terminates in a rounded posterior peak.
10. The knee prosthesis according to claim 8, wherein said posterior cam has a length from an anterior end to a posterior end that is substantially equal to the length of said curved surface of said posterior face of said spine.
11. The knee prosthesis according to claim 1, wherein said cam housing defines an anterior-posterior distance between said curved surface of said posterior cam at said one end and an opposite end of said cam housing that is substantially greater than an anterior-posterior dimension of said spine.
12. The knee prosthesis according to claim 11, wherein the anterior-posterior distance defined by said cam housing is about 1.5 times greater than the anterior-posterior dimension of said spine.
13. The knee prosthesis according to claim 1, wherein said bearing is mounted on said platform to permit relative movement therebetween.
14. The knee prosthesis according to claim 13, wherein said tibial component includes:
a socket defined in said platform; and
a stem extending from said bearing configured for rotating engagement within said socket.
15. A knee prosthesis comprising:
a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, said notch defining an elongated cam housing having a posterior cam at one end of said cam housing;
a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on said platform, said bearing defining medial and lateral bearing surfaces configured to articulate with said medial and lateral condyle surfaces, and a spine projecting superiorly within said cam housing when said condyle surfaces are in articulating contact with said bearing surfaces, wherein said spine defines a posterior face facing said posterior cam and configured for cooperative engagement when said posterior cam, said spine further defining a bore therethrough; and
a pin configured to be disposed within said bore, said pin formed of a material different from the material of said spine.
16. The knee prosthesis according to claim 15, wherein said pin is configured to be press-fit into said bore.
17. The knee prosthesis according to claim 15, wherein tibial component includes:
a socket defined in said platform; and
a stem extending from said bearing configured for rotating engagement within said socket.
18. The knee prosthesis according to claim 17, wherein said bore extends into at least a portion of said stem and said pin is configured to extend into said portion of said stem.
19. The knee prosthesis according to claim 15, wherein said pin is formed of a mechanically stiffer material than said spine.
20. The knee prosthesis according to claim 19, wherein said spine is formed of a plastic and said pin is formed of a metal.
21. A knee prosthesis comprising:
a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, said notch defining an elongated cam housing having an anterior cam and a posterior cam at opposite ends of said cam housing; and
a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on said platform, said bearing defining medial and lateral bearing surfaces configured for rotating contact with said medial and lateral condyle surfaces, and a spine projecting superiorly from said bearing within said cam housing when said condyle surfaces are in articulating contact with said bearing surfaces, and said spine defining an anterior face facing said anterior cam and a posterior face adapted for articulating contact with said posterior cam,
wherein said cam housing is configured to define an anterior-posterior distance between said anterior cam and said posterior face of said spine when said femoral component and said tibial component are in a normally extended position relative to each other, whereby said posterior face of said spine is in articulating contact with said posterior cam only at a first predetermined flexion rotation angle between said femoral component and said tibial component.
22. The knee prosthesis according to claim 21, wherein said first predetermined flexion angle is about 50°.
23. The knee prosthesis according to claim 21, wherein said posterior cam and said posterior face define complementary curved surfaces, whereby said complementary surfaces articulate relative to each other at flexion angles between said femoral component and said tibial component greater than said first predetermined flexion angle.
24. The knee prosthesis according to claim 23, wherein said posterior cam includes a rounded anterior end that is arranged to contact said posterior face first at said first predetermined flexion angle.
25. The knee prosthesis according to claim 23, wherein the complementary curved surface of said posterior cam is arranged on said posterior cam so that complementary curved surface of said posterior cam is substantially nested within the complementary curved surface of said posterior face of said spine only after said femoral component and said tibial component rotate relative to each other to a second predetermined flexion angle greater than said first predetermined flexion angle.
26. A knee prosthesis, comprising:
a femoral component configured to be attached to the distal end of a femur and having a medial and a lateral condyle surface spaced apart to define a notch therebetween, said notch defining an elongated cam housing having a posterior cam at one end thereof; and
a tibial component including a platform configured for attachment to the proximal end of a tibia and a bearing supported on said platform, said bearing defining medial and lateral bearing surfaces configured for rotating contact with said medial and lateral condyle surfaces, and a spine projecting superiorly from said bearing within said cam housing when said condyle surfaces are in articulating contact with said bearing surfaces, and said spine defining a posterior face adapted for articulating contact with said posterior cam,
wherein the rotating contact between said bearing and said condyle surfaces is configured to carry all of the anterior-posterior shear load of the knee prosthesis from a full extension angle to a predetermined flexion angle between said femoral component and said tibial component, and said spine is arranged relative to the rotating contact between said bearing and said condyle surfaces so that said spine contacts said posterior cam at said predetermined flexion angle to share a portion of the anterior posterior shear load of the knee at flexion angles greater than said predetermined flexion angle.
US10/242,122 2002-09-12 2002-09-12 Posterior stabilized knee with varus-valgus constraint Abandoned US20040054416A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US10/242,122 US20040054416A1 (en) 2002-09-12 2002-09-12 Posterior stabilized knee with varus-valgus constraint
DE60305115T DE60305115T2 (en) 2002-09-12 2003-09-09 Posterior stabilized knee prosthesis with varus / valgus restriction
AT03255592T ATE325587T1 (en) 2002-09-12 2003-09-09 POSTERIOR STABILIZED KNEE PROSTHESIS WITH VARUS/VALGUS RESTRICTION
ES03255592T ES2263923T3 (en) 2002-09-12 2003-09-09 BACK KNEE PROTESIS WITH CONSTRUCTION IN VARO-VALGO.
AU2003244616A AU2003244616B2 (en) 2002-09-12 2003-09-09 Posterior stabilized knee with varus-valgus constraint
DK03255592T DK1400220T3 (en) 2002-09-12 2003-09-09 Posterior stabilized knee with varus-valgus constraint
EP03255592A EP1400220B1 (en) 2002-09-12 2003-09-09 Posterior stabilized knee with varus-valgus constraint
US11/121,408 US8382847B2 (en) 2002-09-12 2005-05-04 Posterior stabilized knee with varus-valgus constraint
US13/763,305 US20130150976A1 (en) 2002-09-12 2013-02-08 Posterior Stabilized Knee With Varus-Valgus Constraint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10/242,122 US20040054416A1 (en) 2002-09-12 2002-09-12 Posterior stabilized knee with varus-valgus constraint

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/121,408 Continuation US8382847B2 (en) 2002-09-12 2005-05-04 Posterior stabilized knee with varus-valgus constraint

Publications (1)

Publication Number Publication Date
US20040054416A1 true US20040054416A1 (en) 2004-03-18

Family

ID=31946380

Family Applications (3)

Application Number Title Priority Date Filing Date
US10/242,122 Abandoned US20040054416A1 (en) 2002-09-12 2002-09-12 Posterior stabilized knee with varus-valgus constraint
US11/121,408 Active 2029-02-19 US8382847B2 (en) 2002-09-12 2005-05-04 Posterior stabilized knee with varus-valgus constraint
US13/763,305 Abandoned US20130150976A1 (en) 2002-09-12 2013-02-08 Posterior Stabilized Knee With Varus-Valgus Constraint

Family Applications After (2)

Application Number Title Priority Date Filing Date
US11/121,408 Active 2029-02-19 US8382847B2 (en) 2002-09-12 2005-05-04 Posterior stabilized knee with varus-valgus constraint
US13/763,305 Abandoned US20130150976A1 (en) 2002-09-12 2013-02-08 Posterior Stabilized Knee With Varus-Valgus Constraint

Country Status (7)

Country Link
US (3) US20040054416A1 (en)
EP (1) EP1400220B1 (en)
AT (1) ATE325587T1 (en)
AU (1) AU2003244616B2 (en)
DE (1) DE60305115T2 (en)
DK (1) DK1400220T3 (en)
ES (1) ES2263923T3 (en)

Cited By (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040191106A1 (en) * 2002-11-08 2004-09-30 Howmedica Osteonics Corp. Laser-produced porous surface
US20050143832A1 (en) * 2003-10-17 2005-06-30 Carson Christopher P. High flexion articular insert
US20050203629A1 (en) * 2004-02-26 2005-09-15 George Cipolletti Modular knee prosthesis
US20050278035A1 (en) * 2004-06-11 2005-12-15 Wyss Joseph G Posterior stabilized mobile bearing knee
US20060147332A1 (en) * 2004-12-30 2006-07-06 Howmedica Osteonics Corp. Laser-produced porous structure
US20070135926A1 (en) * 2005-12-14 2007-06-14 Peter Walker Surface guided knee replacement
US20080050412A1 (en) * 2006-08-15 2008-02-28 Howmedica Osteonics Corp. Antimicrobial implant
US20090088860A1 (en) * 2007-09-30 2009-04-02 Romeis Kristen L Hinged orthopaedic prosthesis
US20090319049A1 (en) * 2008-02-18 2009-12-24 Maxx Orthopedics, Inc. Total Knee Replacement Prosthesis With High Order NURBS Surfaces
US20100234962A1 (en) * 2001-01-29 2010-09-16 Zimmer Technology, Inc. Constrained prosthetic knee with rotating bearing
US8142886B2 (en) 2007-07-24 2012-03-27 Howmedica Osteonics Corp. Porous laser sintered articles
US8403994B2 (en) 2011-01-19 2013-03-26 Wright Medical Technology, Inc. Knee implant system
US20130158671A1 (en) * 2007-04-17 2013-06-20 Biomet Manufacturing Corp. Method And Apparatus For Manufacturing An Implant
USRE44476E1 (en) 2001-01-29 2013-09-03 Zimmer, Inc. Constrained prosthetic knee with rotating bearing
US8556981B2 (en) 2005-12-06 2013-10-15 Howmedica Osteonics Corp. Laser-produced porous surface
US20140114427A1 (en) * 2011-06-17 2014-04-24 Biomet Manufacturing, Llc Revision knee tibial locking mechanism
JP2014510562A (en) * 2011-01-27 2014-05-01 スミス アンド ネフュー インコーポレーテッド Restraint knee prosthesis
US8979936B2 (en) 2006-06-09 2015-03-17 Biomet Manufacturing, Llc Patient-modified implant
US9005297B2 (en) 2006-02-27 2015-04-14 Biomet Manufacturing, Llc Patient-specific elbow guides and associated methods
US9084618B2 (en) 2011-06-13 2015-07-21 Biomet Manufacturing, Llc Drill guides for confirming alignment of patient-specific alignment guides
US9113971B2 (en) 2006-02-27 2015-08-25 Biomet Manufacturing, Llc Femoral acetabular impingement guide
US9135374B2 (en) 2012-04-06 2015-09-15 Howmedica Osteonics Corp. Surface modified unit cell lattice structures for optimized secure freeform fabrication
US9173666B2 (en) 2011-07-01 2015-11-03 Biomet Manufacturing, Llc Patient-specific-bone-cutting guidance instruments and methods
US9180010B2 (en) 2012-04-06 2015-11-10 Howmedica Osteonics Corp. Surface modified unit cell lattice structures for optimized secure freeform fabrication
US9204977B2 (en) 2012-12-11 2015-12-08 Biomet Manufacturing, Llc Patient-specific acetabular guide for anterior approach
US9237950B2 (en) 2012-02-02 2016-01-19 Biomet Manufacturing, Llc Implant with patient-specific porous structure
US9241745B2 (en) 2011-03-07 2016-01-26 Biomet Manufacturing, Llc Patient-specific femoral version guide
US9271744B2 (en) 2010-09-29 2016-03-01 Biomet Manufacturing, Llc Patient-specific guide for partial acetabular socket replacement
US9289253B2 (en) 2006-02-27 2016-03-22 Biomet Manufacturing, Llc Patient-specific shoulder guide
US9295497B2 (en) 2011-08-31 2016-03-29 Biomet Manufacturing, Llc Patient-specific sacroiliac and pedicle guides
US9301812B2 (en) 2011-10-27 2016-04-05 Biomet Manufacturing, Llc Methods for patient-specific shoulder arthroplasty
US9339278B2 (en) 2006-02-27 2016-05-17 Biomet Manufacturing, Llc Patient-specific acetabular guides and associated instruments
US9345548B2 (en) 2006-02-27 2016-05-24 Biomet Manufacturing, Llc Patient-specific pre-operative planning
US9351743B2 (en) 2011-10-27 2016-05-31 Biomet Manufacturing, Llc Patient-specific glenoid guides
US9364896B2 (en) 2012-02-07 2016-06-14 Medical Modeling Inc. Fabrication of hybrid solid-porous medical implantable devices with electron beam melting technology
US9386993B2 (en) 2011-09-29 2016-07-12 Biomet Manufacturing, Llc Patient-specific femoroacetabular impingement instruments and methods
US9393028B2 (en) 2009-08-13 2016-07-19 Biomet Manufacturing, Llc Device for the resection of bones, method for producing such a device, endoprosthesis suited for this purpose and method for producing such an endoprosthesis
US9408616B2 (en) 2014-05-12 2016-08-09 Biomet Manufacturing, Llc Humeral cut guide
US9427320B2 (en) 2011-08-04 2016-08-30 Biomet Manufacturing, Llc Patient-specific pelvic implants for acetabular reconstruction
US9439659B2 (en) 2011-08-31 2016-09-13 Biomet Manufacturing, Llc Patient-specific sacroiliac guides and associated methods
US9445907B2 (en) 2011-03-07 2016-09-20 Biomet Manufacturing, Llc Patient-specific tools and implants
US9451973B2 (en) 2011-10-27 2016-09-27 Biomet Manufacturing, Llc Patient specific glenoid guide
US9456833B2 (en) 2010-02-26 2016-10-04 Biomet Sports Medicine, Llc Patient-specific osteotomy devices and methods
US9468538B2 (en) 2009-03-24 2016-10-18 Biomet Manufacturing, Llc Method and apparatus for aligning and securing an implant relative to a patient
US9474539B2 (en) 2011-04-29 2016-10-25 Biomet Manufacturing, Llc Patient-specific convertible guides
US9480580B2 (en) 2006-02-27 2016-11-01 Biomet Manufacturing, Llc Patient-specific acetabular alignment guides
US9480490B2 (en) 2006-02-27 2016-11-01 Biomet Manufacturing, Llc Patient-specific guides
US9498233B2 (en) 2013-03-13 2016-11-22 Biomet Manufacturing, Llc. Universal acetabular guide and associated hardware
US9517145B2 (en) 2013-03-15 2016-12-13 Biomet Manufacturing, Llc Guide alignment system and method
US9522010B2 (en) 2006-02-27 2016-12-20 Biomet Manufacturing, Llc Patient-specific orthopedic instruments
US9554910B2 (en) 2011-10-27 2017-01-31 Biomet Manufacturing, Llc Patient-specific glenoid guide and implants
US9561040B2 (en) 2014-06-03 2017-02-07 Biomet Manufacturing, Llc Patient-specific glenoid depth control
US9572590B2 (en) 2006-10-03 2017-02-21 Biomet Uk Limited Surgical instrument
US9579107B2 (en) 2013-03-12 2017-02-28 Biomet Manufacturing, Llc Multi-point fit for patient specific guide
US9662127B2 (en) 2006-02-27 2017-05-30 Biomet Manufacturing, Llc Patient-specific acetabular guides and associated instruments
US9662216B2 (en) 2006-02-27 2017-05-30 Biomet Manufacturing, Llc Patient-specific hip joint devices
US9675400B2 (en) 2011-04-19 2017-06-13 Biomet Manufacturing, Llc Patient-specific fracture fixation instrumentation and method
US9717510B2 (en) 2011-04-15 2017-08-01 Biomet Manufacturing, Llc Patient-specific numerically controlled instrument
US9743940B2 (en) 2011-04-29 2017-08-29 Biomet Manufacturing, Llc Patient-specific partial knee guides and other instruments
US9757238B2 (en) 2011-06-06 2017-09-12 Biomet Manufacturing, Llc Pre-operative planning and manufacturing method for orthopedic procedure
US9795399B2 (en) 2006-06-09 2017-10-24 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US20170325973A1 (en) * 2014-12-11 2017-11-16 Think Surgical, Inc. Surveying tibial trials for knee anthroplasty
US9820868B2 (en) 2015-03-30 2017-11-21 Biomet Manufacturing, Llc Method and apparatus for a pin apparatus
US9826994B2 (en) 2014-09-29 2017-11-28 Biomet Manufacturing, Llc Adjustable glenoid pin insertion guide
US9826981B2 (en) 2013-03-13 2017-11-28 Biomet Manufacturing, Llc Tangential fit of patient-specific guides
US9833245B2 (en) 2014-09-29 2017-12-05 Biomet Sports Medicine, Llc Tibial tubercule osteotomy
US9839436B2 (en) 2014-06-03 2017-12-12 Biomet Manufacturing, Llc Patient-specific glenoid depth control
US9839438B2 (en) 2013-03-11 2017-12-12 Biomet Manufacturing, Llc Patient-specific glenoid guide with a reusable guide holder
US9861387B2 (en) 2006-06-09 2018-01-09 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US9918740B2 (en) 2006-02-27 2018-03-20 Biomet Manufacturing, Llc Backup surgical instrument system and method
US9968376B2 (en) 2010-11-29 2018-05-15 Biomet Manufacturing, Llc Patient-specific orthopedic instruments
US10226262B2 (en) 2015-06-25 2019-03-12 Biomet Manufacturing, Llc Patient-specific humeral guide designs
US10278711B2 (en) 2006-02-27 2019-05-07 Biomet Manufacturing, Llc Patient-specific femoral guide
US10282488B2 (en) 2014-04-25 2019-05-07 Biomet Manufacturing, Llc HTO guide with optional guided ACL/PCL tunnels
US10426492B2 (en) 2006-02-27 2019-10-01 Biomet Manufacturing, Llc Patient specific alignment guide with cutting surface and laser indicator
US10568647B2 (en) 2015-06-25 2020-02-25 Biomet Manufacturing, Llc Patient-specific humeral guide designs
US10603179B2 (en) 2006-02-27 2020-03-31 Biomet Manufacturing, Llc Patient-specific augments
CN111297520A (en) * 2020-03-23 2020-06-19 北京市春立正达医疗器械股份有限公司 Biological type tibial plateau holds in palm and platform pad
US10722310B2 (en) 2017-03-13 2020-07-28 Zimmer Biomet CMF and Thoracic, LLC Virtual surgery planning system and method
US10736748B2 (en) 2018-05-02 2020-08-11 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a hinged-knee prosthesis
US11033396B2 (en) 2019-02-05 2021-06-15 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a rotating hinged-knee prosthesis
US11116641B2 (en) 2019-02-05 2021-09-14 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a rotating hinged-knee prosthesis
US11179165B2 (en) 2013-10-21 2021-11-23 Biomet Manufacturing, Llc Ligament guide registration
US11298747B2 (en) 2017-05-18 2022-04-12 Howmedica Osteonics Corp. High fatigue strength porous structure
US11369477B2 (en) 2002-12-20 2022-06-28 Smith & Nephew, Inc. High performance knee prostheses
US11419618B2 (en) 2011-10-27 2022-08-23 Biomet Manufacturing, Llc Patient-specific glenoid guides
US11554019B2 (en) 2007-04-17 2023-01-17 Biomet Manufacturing, Llc Method and apparatus for manufacturing an implant

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7658767B2 (en) 2006-06-30 2010-02-09 Depuy Products, Inc. Hinged orthopaedic prosthesis
US20080033567A1 (en) * 2006-08-03 2008-02-07 Stchur Robert P Knee joint prosthesis used in total knee arthroplasty
US8632600B2 (en) * 2007-09-25 2014-01-21 Depuy (Ireland) Prosthesis with modular extensions
US9204967B2 (en) * 2007-09-28 2015-12-08 Depuy (Ireland) Fixed-bearing knee prosthesis having interchangeable components
US8828088B2 (en) * 2007-11-08 2014-09-09 Linares Medical Devices, Llc Joint assembly incorporating undercut surface design to entrap accumulating wear debris from plastic joint assembly
US8979938B2 (en) * 2007-11-08 2015-03-17 Linares Medical Devices, Llc Artificial knee implant including liquid ballast supporting / rotating surfaces and incorporating flexible multi-material and natural lubricant retaining matrix applied to a joint surface
WO2009108960A2 (en) 2008-02-25 2009-09-03 Linares Medical Devices, Llc Artificial wear resistant plug for mounting to existing joint bone
US9539097B2 (en) 2007-11-08 2017-01-10 Linares Medical Devices, Llc Hip and knee joint assemblies incorporating debris collection architecture between the ball and seat interface
US8764837B2 (en) * 2008-03-26 2014-07-01 Linares Medical Devices, Llc Reinforced joint assembly
US8075626B2 (en) * 2008-06-30 2011-12-13 Depuy Products, Inc. Orthopaedic knee prosthesis having increased axial-rotation
US8480752B2 (en) 2008-06-30 2013-07-09 DePuy Synthes Products, LLC Tibial bearing having increased axial-rotation
US8491662B2 (en) 2008-12-23 2013-07-23 Aesculap Ag Knee prosthesis
US9220600B2 (en) 2008-12-23 2015-12-29 Aesculap Implant Systems, Llc Knee prosthesis
US20100161067A1 (en) * 2008-12-23 2010-06-24 Aesculap Ag Knee prosthesis
DE202009008370U1 (en) * 2009-06-17 2010-10-28 Lawton Gmbh & Co. Kg Surgical instrument
US9011547B2 (en) 2010-01-21 2015-04-21 Depuy (Ireland) Knee prosthesis system
US8926705B2 (en) 2010-05-10 2015-01-06 Linares Medical Devices, Llc Implantable joint assembly featuring debris entrapment chamber subassemblies along with opposing magnetic fields generated between articulating implant components in order to minimize frictional force and associated wear
US8545571B2 (en) 2010-07-30 2013-10-01 Howmedica Osteonics Corp. Stabilized knee prosthesis
CN103997978A (en) * 2011-07-13 2014-08-20 通用医疗公司 Methods and devices for knee joint replacement with anterior cruciate ligament substitution
CN110432961B (en) * 2019-07-19 2021-07-09 温州医科大学附属第一医院 Tibial plateau fracture piece wicresoft restorer that sinks

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298992A (en) * 1980-01-21 1981-11-10 New York Society For The Relief Of The Ruptured And Crippled Posteriorly stabilized total knee joint prosthesis
US4634444A (en) * 1984-02-09 1987-01-06 Joint Medical Products Corporation Semi-constrained artificial joint
US5007932A (en) * 1985-01-08 1991-04-16 Ngk Spark Plug Co., Ltd. Artificial bone joint
US5116375A (en) * 1990-08-27 1992-05-26 Hofmann Aaron A Knee prosthesis
US5147405A (en) * 1990-02-07 1992-09-15 Boehringer Mannheim Corporation Knee prosthesis
US5330532A (en) * 1990-11-09 1994-07-19 Chitranjan Ranawat Knee joint prosthesis
US5549686A (en) * 1994-06-06 1996-08-27 Zimmer, Inc. Knee prosthesis having a tapered cam
US5658342A (en) * 1992-11-16 1997-08-19 Arch Development Stabilized prosthetic knee
US6123729A (en) * 1998-03-10 2000-09-26 Bristol-Myers Squibb Company Four compartment knee
US6203576B1 (en) * 1996-12-09 2001-03-20 Groupe Controle Dedienne Gcd Societe De Droit Francais Complete knee joint prosthesis
US6325828B1 (en) * 1997-12-02 2001-12-04 Rose Biomedical Research Apparatus for knee prosthesis
US6406497B2 (en) * 2000-07-19 2002-06-18 Tsunenori Takei Artificial knee joint
US6475241B2 (en) * 2000-03-13 2002-11-05 Biomedical Engineering Trust I Posterior stabilized knee replacement with bearing translation for knees with retained collateral ligaments
US20030009232A1 (en) * 1999-03-01 2003-01-09 Robert Metzger Floating bearing knee joint prosthesis with a fixed tibial post
US6558426B1 (en) * 2000-11-28 2003-05-06 Medidea, Llc Multiple-cam, posterior-stabilized knee prosthesis
US6620198B2 (en) * 1999-10-07 2003-09-16 Exactech, Inc. Composite bearing inserts for total knee joints
US6699291B1 (en) * 1999-04-01 2004-03-02 Merck Biomaterial France Antero-postero-stabilized knee prosthesis

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5011496A (en) * 1988-02-02 1991-04-30 Joint Medical Products Corporation Prosthetic joint
US5330534A (en) * 1992-02-10 1994-07-19 Biomet, Inc. Knee joint prosthesis with interchangeable components
US5370699A (en) * 1993-01-21 1994-12-06 Orthomet, Inc. Modular knee joint prosthesis
US6039764A (en) * 1997-08-18 2000-03-21 Arch Development Corporation Prosthetic knee with adjusted center of internal/external rotation
US6206926B1 (en) 1997-10-06 2001-03-27 Biomedical Engineering Trust I Prosthetic knee joint with enhanced posterior stabilization and dislocation prevention features
US6443991B1 (en) 1998-09-21 2002-09-03 Depuy Orthopaedics, Inc. Posterior stabilized mobile bearing knee
FR2805456B1 (en) * 2000-02-28 2002-12-06 Groupe Lepine TOTAL KNEE PROSTHESIS, OF THE TYPE SAID "POSTERO-STABILIZED"
US20040002767A1 (en) * 2002-06-28 2004-01-01 Joseph Wyss Modular knee joint prosthesis

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298992A (en) * 1980-01-21 1981-11-10 New York Society For The Relief Of The Ruptured And Crippled Posteriorly stabilized total knee joint prosthesis
US4634444A (en) * 1984-02-09 1987-01-06 Joint Medical Products Corporation Semi-constrained artificial joint
US5007932A (en) * 1985-01-08 1991-04-16 Ngk Spark Plug Co., Ltd. Artificial bone joint
US5147405A (en) * 1990-02-07 1992-09-15 Boehringer Mannheim Corporation Knee prosthesis
US5116375A (en) * 1990-08-27 1992-05-26 Hofmann Aaron A Knee prosthesis
US5330532A (en) * 1990-11-09 1994-07-19 Chitranjan Ranawat Knee joint prosthesis
US5658342A (en) * 1992-11-16 1997-08-19 Arch Development Stabilized prosthetic knee
US5549686A (en) * 1994-06-06 1996-08-27 Zimmer, Inc. Knee prosthesis having a tapered cam
US6203576B1 (en) * 1996-12-09 2001-03-20 Groupe Controle Dedienne Gcd Societe De Droit Francais Complete knee joint prosthesis
US6325828B1 (en) * 1997-12-02 2001-12-04 Rose Biomedical Research Apparatus for knee prosthesis
US6123729A (en) * 1998-03-10 2000-09-26 Bristol-Myers Squibb Company Four compartment knee
US20030009232A1 (en) * 1999-03-01 2003-01-09 Robert Metzger Floating bearing knee joint prosthesis with a fixed tibial post
US6699291B1 (en) * 1999-04-01 2004-03-02 Merck Biomaterial France Antero-postero-stabilized knee prosthesis
US6620198B2 (en) * 1999-10-07 2003-09-16 Exactech, Inc. Composite bearing inserts for total knee joints
US6475241B2 (en) * 2000-03-13 2002-11-05 Biomedical Engineering Trust I Posterior stabilized knee replacement with bearing translation for knees with retained collateral ligaments
US6406497B2 (en) * 2000-07-19 2002-06-18 Tsunenori Takei Artificial knee joint
US6558426B1 (en) * 2000-11-28 2003-05-06 Medidea, Llc Multiple-cam, posterior-stabilized knee prosthesis

Cited By (168)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8888857B2 (en) 2001-01-29 2014-11-18 Zimmer, Inc. Constrained prosthetic knee with rotating bearing
USRE44476E1 (en) 2001-01-29 2013-09-03 Zimmer, Inc. Constrained prosthetic knee with rotating bearing
US8268006B2 (en) * 2001-01-29 2012-09-18 Zimmer, Inc. Constrained prosthetic knee with rotating bearing
US20100234962A1 (en) * 2001-01-29 2010-09-16 Zimmer Technology, Inc. Constrained prosthetic knee with rotating bearing
US8992703B2 (en) 2002-11-08 2015-03-31 Howmedica Osteonics Corp. Laser-produced porous surface
US8268099B2 (en) 2002-11-08 2012-09-18 Howmedica Osteonics Corp. Laser-produced porous surface
US20040191106A1 (en) * 2002-11-08 2004-09-30 Howmedica Osteonics Corp. Laser-produced porous surface
US11155073B2 (en) 2002-11-08 2021-10-26 Howmedica Osteonics Corp. Laser-produced porous surface
US10525688B2 (en) 2002-11-08 2020-01-07 Howmedica Osteonics Corp. Laser-produced porous surface
US8268100B2 (en) 2002-11-08 2012-09-18 Howmedica Osteonics Corp. Laser-produced porous surface
US11510783B2 (en) 2002-11-08 2022-11-29 Howmedica Osteonics Corp. Laser-produced porous surface
US11186077B2 (en) 2002-11-08 2021-11-30 Howmedica Osteonics Corp. Laser-produced porous surface
US11369477B2 (en) 2002-12-20 2022-06-28 Smith & Nephew, Inc. High performance knee prostheses
US9642711B2 (en) 2003-10-17 2017-05-09 Smith & Nephew, Inc. High flexion articular insert
US20050143832A1 (en) * 2003-10-17 2005-06-30 Carson Christopher P. High flexion articular insert
US20100262253A1 (en) * 2004-02-26 2010-10-14 Omni Life Science, Inc. Modular Knee Prosthesis
US7753960B2 (en) * 2004-02-26 2010-07-13 Omni Life Science, Inc. Modular knee prosthesis
US8277513B2 (en) 2004-02-26 2012-10-02 Omni Life Science, Inc. Modular knee prosthesis
US20050203629A1 (en) * 2004-02-26 2005-09-15 George Cipolletti Modular knee prosthesis
US7731755B2 (en) 2004-06-11 2010-06-08 Depuy Products, Inc. Posterior stabilized mobile bearing knee
US20050278035A1 (en) * 2004-06-11 2005-12-15 Wyss Joseph G Posterior stabilized mobile bearing knee
US9456901B2 (en) 2004-12-30 2016-10-04 Howmedica Osteonics Corp. Laser-produced porous structure
US20060147332A1 (en) * 2004-12-30 2006-07-06 Howmedica Osteonics Corp. Laser-produced porous structure
US11660195B2 (en) 2004-12-30 2023-05-30 Howmedica Osteonics Corp. Laser-produced porous structure
US8556981B2 (en) 2005-12-06 2013-10-15 Howmedica Osteonics Corp. Laser-produced porous surface
US8728387B2 (en) 2005-12-06 2014-05-20 Howmedica Osteonics Corp. Laser-produced porous surface
US11918474B2 (en) 2005-12-06 2024-03-05 The University Of Liverpool Laser-produced porous surface
US10398559B2 (en) 2005-12-06 2019-09-03 Howmedica Osteonics Corp. Laser-produced porous surface
US10716673B2 (en) 2005-12-06 2020-07-21 Howmedica Osteonics Corp. Laser-produced porous surface
US8211181B2 (en) * 2005-12-14 2012-07-03 New York University Surface guided knee replacement
US20070135926A1 (en) * 2005-12-14 2007-06-14 Peter Walker Surface guided knee replacement
US9480490B2 (en) 2006-02-27 2016-11-01 Biomet Manufacturing, Llc Patient-specific guides
US9913734B2 (en) 2006-02-27 2018-03-13 Biomet Manufacturing, Llc Patient-specific acetabular alignment guides
US9113971B2 (en) 2006-02-27 2015-08-25 Biomet Manufacturing, Llc Femoral acetabular impingement guide
US9522010B2 (en) 2006-02-27 2016-12-20 Biomet Manufacturing, Llc Patient-specific orthopedic instruments
US10426492B2 (en) 2006-02-27 2019-10-01 Biomet Manufacturing, Llc Patient specific alignment guide with cutting surface and laser indicator
US11534313B2 (en) 2006-02-27 2022-12-27 Biomet Manufacturing, Llc Patient-specific pre-operative planning
US9005297B2 (en) 2006-02-27 2015-04-14 Biomet Manufacturing, Llc Patient-specific elbow guides and associated methods
US10507029B2 (en) 2006-02-27 2019-12-17 Biomet Manufacturing, Llc Patient-specific acetabular guides and associated instruments
US9539013B2 (en) 2006-02-27 2017-01-10 Biomet Manufacturing, Llc Patient-specific elbow guides and associated methods
US9480580B2 (en) 2006-02-27 2016-11-01 Biomet Manufacturing, Llc Patient-specific acetabular alignment guides
US9289253B2 (en) 2006-02-27 2016-03-22 Biomet Manufacturing, Llc Patient-specific shoulder guide
US9918740B2 (en) 2006-02-27 2018-03-20 Biomet Manufacturing, Llc Backup surgical instrument system and method
US10390845B2 (en) 2006-02-27 2019-08-27 Biomet Manufacturing, Llc Patient-specific shoulder guide
US9339278B2 (en) 2006-02-27 2016-05-17 Biomet Manufacturing, Llc Patient-specific acetabular guides and associated instruments
US9345548B2 (en) 2006-02-27 2016-05-24 Biomet Manufacturing, Llc Patient-specific pre-operative planning
US10278711B2 (en) 2006-02-27 2019-05-07 Biomet Manufacturing, Llc Patient-specific femoral guide
US10603179B2 (en) 2006-02-27 2020-03-31 Biomet Manufacturing, Llc Patient-specific augments
US9700329B2 (en) 2006-02-27 2017-07-11 Biomet Manufacturing, Llc Patient-specific orthopedic instruments
US9662127B2 (en) 2006-02-27 2017-05-30 Biomet Manufacturing, Llc Patient-specific acetabular guides and associated instruments
US10206695B2 (en) 2006-02-27 2019-02-19 Biomet Manufacturing, Llc Femoral acetabular impingement guide
US9662216B2 (en) 2006-02-27 2017-05-30 Biomet Manufacturing, Llc Patient-specific hip joint devices
US10743937B2 (en) 2006-02-27 2020-08-18 Biomet Manufacturing, Llc Backup surgical instrument system and method
US10206697B2 (en) 2006-06-09 2019-02-19 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US11576689B2 (en) 2006-06-09 2023-02-14 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US9861387B2 (en) 2006-06-09 2018-01-09 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US8979936B2 (en) 2006-06-09 2015-03-17 Biomet Manufacturing, Llc Patient-modified implant
US10893879B2 (en) 2006-06-09 2021-01-19 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US9993344B2 (en) 2006-06-09 2018-06-12 Biomet Manufacturing, Llc Patient-modified implant
US9795399B2 (en) 2006-06-09 2017-10-24 Biomet Manufacturing, Llc Patient-specific knee alignment guide and associated method
US8147861B2 (en) 2006-08-15 2012-04-03 Howmedica Osteonics Corp. Antimicrobial implant
US20080050412A1 (en) * 2006-08-15 2008-02-28 Howmedica Osteonics Corp. Antimicrobial implant
US9572590B2 (en) 2006-10-03 2017-02-21 Biomet Uk Limited Surgical instrument
US11554019B2 (en) 2007-04-17 2023-01-17 Biomet Manufacturing, Llc Method and apparatus for manufacturing an implant
US20130158671A1 (en) * 2007-04-17 2013-06-20 Biomet Manufacturing Corp. Method And Apparatus For Manufacturing An Implant
US8142886B2 (en) 2007-07-24 2012-03-27 Howmedica Osteonics Corp. Porous laser sintered articles
US20090088860A1 (en) * 2007-09-30 2009-04-02 Romeis Kristen L Hinged orthopaedic prosthesis
US7918893B2 (en) * 2007-09-30 2011-04-05 Depuy Products, Inc. Hinged orthopaedic prosthesis
US9788955B2 (en) * 2008-02-18 2017-10-17 Maxx Orthopedics, Inc. Total knee replacement prosthesis with high order NURBS surfaces
US20090319049A1 (en) * 2008-02-18 2009-12-24 Maxx Orthopedics, Inc. Total Knee Replacement Prosthesis With High Order NURBS Surfaces
US10159498B2 (en) * 2008-04-16 2018-12-25 Biomet Manufacturing, Llc Method and apparatus for manufacturing an implant
US9468538B2 (en) 2009-03-24 2016-10-18 Biomet Manufacturing, Llc Method and apparatus for aligning and securing an implant relative to a patient
US9839433B2 (en) 2009-08-13 2017-12-12 Biomet Manufacturing, Llc Device for the resection of bones, method for producing such a device, endoprosthesis suited for this purpose and method for producing such an endoprosthesis
US10052110B2 (en) 2009-08-13 2018-08-21 Biomet Manufacturing, Llc Device for the resection of bones, method for producing such a device, endoprosthesis suited for this purpose and method for producing such an endoprosthesis
US9393028B2 (en) 2009-08-13 2016-07-19 Biomet Manufacturing, Llc Device for the resection of bones, method for producing such a device, endoprosthesis suited for this purpose and method for producing such an endoprosthesis
US11324522B2 (en) 2009-10-01 2022-05-10 Biomet Manufacturing, Llc Patient specific alignment guide with cutting surface and laser indicator
US9456833B2 (en) 2010-02-26 2016-10-04 Biomet Sports Medicine, Llc Patient-specific osteotomy devices and methods
US10893876B2 (en) 2010-03-05 2021-01-19 Biomet Manufacturing, Llc Method and apparatus for manufacturing an implant
US9271744B2 (en) 2010-09-29 2016-03-01 Biomet Manufacturing, Llc Patient-specific guide for partial acetabular socket replacement
US10098648B2 (en) 2010-09-29 2018-10-16 Biomet Manufacturing, Llc Patient-specific guide for partial acetabular socket replacement
US11234719B2 (en) 2010-11-03 2022-02-01 Biomet Manufacturing, Llc Patient-specific shoulder guide
US9968376B2 (en) 2010-11-29 2018-05-15 Biomet Manufacturing, Llc Patient-specific orthopedic instruments
US9381088B2 (en) 2011-01-19 2016-07-05 Microport Orthopedics Holdings Inc. Knee implant system
US8403994B2 (en) 2011-01-19 2013-03-26 Wright Medical Technology, Inc. Knee implant system
JP2014510562A (en) * 2011-01-27 2014-05-01 スミス アンド ネフュー インコーポレーテッド Restraint knee prosthesis
JP2018001001A (en) * 2011-01-27 2018-01-11 スミス アンド ネフュー インコーポレイテッド Constrained knee prosthesis
JP2016163771A (en) * 2011-01-27 2016-09-08 スミス アンド ネフュー インコーポレーテッド Constrained knee prosthesis
US10702389B2 (en) 2011-01-27 2020-07-07 Smith & Nephew, Inc. Knee prosthesis
US9999511B2 (en) 2011-01-27 2018-06-19 Smith & Nephew, Inc. Knee prosthesis
US9743935B2 (en) 2011-03-07 2017-08-29 Biomet Manufacturing, Llc Patient-specific femoral version guide
US9241745B2 (en) 2011-03-07 2016-01-26 Biomet Manufacturing, Llc Patient-specific femoral version guide
US9445907B2 (en) 2011-03-07 2016-09-20 Biomet Manufacturing, Llc Patient-specific tools and implants
US9717510B2 (en) 2011-04-15 2017-08-01 Biomet Manufacturing, Llc Patient-specific numerically controlled instrument
US10251690B2 (en) 2011-04-19 2019-04-09 Biomet Manufacturing, Llc Patient-specific fracture fixation instrumentation and method
US9675400B2 (en) 2011-04-19 2017-06-13 Biomet Manufacturing, Llc Patient-specific fracture fixation instrumentation and method
US9743940B2 (en) 2011-04-29 2017-08-29 Biomet Manufacturing, Llc Patient-specific partial knee guides and other instruments
US9474539B2 (en) 2011-04-29 2016-10-25 Biomet Manufacturing, Llc Patient-specific convertible guides
US9757238B2 (en) 2011-06-06 2017-09-12 Biomet Manufacturing, Llc Pre-operative planning and manufacturing method for orthopedic procedure
US9084618B2 (en) 2011-06-13 2015-07-21 Biomet Manufacturing, Llc Drill guides for confirming alignment of patient-specific alignment guides
US9687261B2 (en) 2011-06-13 2017-06-27 Biomet Manufacturing, Llc Drill guides for confirming alignment of patient-specific alignment guides
US20140114427A1 (en) * 2011-06-17 2014-04-24 Biomet Manufacturing, Llc Revision knee tibial locking mechanism
US9408704B2 (en) * 2011-06-17 2016-08-09 Biomet Manufacturing, Llc Revision knee tibial locking mechanism
US9668747B2 (en) 2011-07-01 2017-06-06 Biomet Manufacturing, Llc Patient-specific-bone-cutting guidance instruments and methods
US9173666B2 (en) 2011-07-01 2015-11-03 Biomet Manufacturing, Llc Patient-specific-bone-cutting guidance instruments and methods
US9427320B2 (en) 2011-08-04 2016-08-30 Biomet Manufacturing, Llc Patient-specific pelvic implants for acetabular reconstruction
US9295497B2 (en) 2011-08-31 2016-03-29 Biomet Manufacturing, Llc Patient-specific sacroiliac and pedicle guides
US9439659B2 (en) 2011-08-31 2016-09-13 Biomet Manufacturing, Llc Patient-specific sacroiliac guides and associated methods
US9603613B2 (en) 2011-08-31 2017-03-28 Biomet Manufacturing, Llc Patient-specific sacroiliac guides and associated methods
US11406398B2 (en) 2011-09-29 2022-08-09 Biomet Manufacturing, Llc Patient-specific femoroacetabular impingement instruments and methods
US9386993B2 (en) 2011-09-29 2016-07-12 Biomet Manufacturing, Llc Patient-specific femoroacetabular impingement instruments and methods
US10456205B2 (en) 2011-09-29 2019-10-29 Biomet Manufacturing, Llc Patient-specific femoroacetabular impingement instruments and methods
US10426549B2 (en) 2011-10-27 2019-10-01 Biomet Manufacturing, Llc Methods for patient-specific shoulder arthroplasty
US9936962B2 (en) 2011-10-27 2018-04-10 Biomet Manufacturing, Llc Patient specific glenoid guide
US9351743B2 (en) 2011-10-27 2016-05-31 Biomet Manufacturing, Llc Patient-specific glenoid guides
US9301812B2 (en) 2011-10-27 2016-04-05 Biomet Manufacturing, Llc Methods for patient-specific shoulder arthroplasty
US9451973B2 (en) 2011-10-27 2016-09-27 Biomet Manufacturing, Llc Patient specific glenoid guide
US11602360B2 (en) 2011-10-27 2023-03-14 Biomet Manufacturing, Llc Patient specific glenoid guide
US9554910B2 (en) 2011-10-27 2017-01-31 Biomet Manufacturing, Llc Patient-specific glenoid guide and implants
US11419618B2 (en) 2011-10-27 2022-08-23 Biomet Manufacturing, Llc Patient-specific glenoid guides
US11298188B2 (en) 2011-10-27 2022-04-12 Biomet Manufacturing, Llc Methods for patient-specific shoulder arthroplasty
US10842510B2 (en) 2011-10-27 2020-11-24 Biomet Manufacturing, Llc Patient specific glenoid guide
US10426493B2 (en) 2011-10-27 2019-10-01 Biomet Manufacturing, Llc Patient-specific glenoid guides
US9237950B2 (en) 2012-02-02 2016-01-19 Biomet Manufacturing, Llc Implant with patient-specific porous structure
US9827106B2 (en) 2012-02-02 2017-11-28 Biomet Manufacturing, Llc Implant with patient-specific porous structure
US9364896B2 (en) 2012-02-07 2016-06-14 Medical Modeling Inc. Fabrication of hybrid solid-porous medical implantable devices with electron beam melting technology
US9135374B2 (en) 2012-04-06 2015-09-15 Howmedica Osteonics Corp. Surface modified unit cell lattice structures for optimized secure freeform fabrication
US9180010B2 (en) 2012-04-06 2015-11-10 Howmedica Osteonics Corp. Surface modified unit cell lattice structures for optimized secure freeform fabrication
US11759323B2 (en) 2012-04-06 2023-09-19 Howmedica Osteonics Corp. Surface modified unit cell lattice structures for optimized secure freeform fabrication
US10614176B2 (en) 2012-04-06 2020-04-07 Howmedica Osteonics Corp. Surface modified unit cell lattice structures for optimized secure freeform fabrication
US9204977B2 (en) 2012-12-11 2015-12-08 Biomet Manufacturing, Llc Patient-specific acetabular guide for anterior approach
US9597201B2 (en) 2012-12-11 2017-03-21 Biomet Manufacturing, Llc Patient-specific acetabular guide for anterior approach
US11617591B2 (en) 2013-03-11 2023-04-04 Biomet Manufacturing, Llc Patient-specific glenoid guide with a reusable guide holder
US10441298B2 (en) 2013-03-11 2019-10-15 Biomet Manufacturing, Llc Patient-specific glenoid guide with a reusable guide holder
US9839438B2 (en) 2013-03-11 2017-12-12 Biomet Manufacturing, Llc Patient-specific glenoid guide with a reusable guide holder
US9700325B2 (en) 2013-03-12 2017-07-11 Biomet Manufacturing, Llc Multi-point fit for patient specific guide
US9579107B2 (en) 2013-03-12 2017-02-28 Biomet Manufacturing, Llc Multi-point fit for patient specific guide
US9498233B2 (en) 2013-03-13 2016-11-22 Biomet Manufacturing, Llc. Universal acetabular guide and associated hardware
US10426491B2 (en) 2013-03-13 2019-10-01 Biomet Manufacturing, Llc Tangential fit of patient-specific guides
US10376270B2 (en) 2013-03-13 2019-08-13 Biomet Manufacturing, Llc Universal acetabular guide and associated hardware
US11191549B2 (en) 2013-03-13 2021-12-07 Biomet Manufacturing, Llc Tangential fit of patient-specific guides
US9826981B2 (en) 2013-03-13 2017-11-28 Biomet Manufacturing, Llc Tangential fit of patient-specific guides
US9517145B2 (en) 2013-03-15 2016-12-13 Biomet Manufacturing, Llc Guide alignment system and method
US11179165B2 (en) 2013-10-21 2021-11-23 Biomet Manufacturing, Llc Ligament guide registration
US10282488B2 (en) 2014-04-25 2019-05-07 Biomet Manufacturing, Llc HTO guide with optional guided ACL/PCL tunnels
US9408616B2 (en) 2014-05-12 2016-08-09 Biomet Manufacturing, Llc Humeral cut guide
US9561040B2 (en) 2014-06-03 2017-02-07 Biomet Manufacturing, Llc Patient-specific glenoid depth control
US9839436B2 (en) 2014-06-03 2017-12-12 Biomet Manufacturing, Llc Patient-specific glenoid depth control
US11026699B2 (en) 2014-09-29 2021-06-08 Biomet Manufacturing, Llc Tibial tubercule osteotomy
US9833245B2 (en) 2014-09-29 2017-12-05 Biomet Sports Medicine, Llc Tibial tubercule osteotomy
US9826994B2 (en) 2014-09-29 2017-11-28 Biomet Manufacturing, Llc Adjustable glenoid pin insertion guide
US10335162B2 (en) 2014-09-29 2019-07-02 Biomet Sports Medicine, Llc Tibial tubercle osteotomy
US10765533B2 (en) * 2014-12-11 2020-09-08 Think Surgical, Inc. Surveying tibial trials for knee arthroplasty
US11744719B2 (en) 2014-12-11 2023-09-05 Think Surgical, Inc. Tibial trial for joint arthroplasty
US20170325973A1 (en) * 2014-12-11 2017-11-16 Think Surgical, Inc. Surveying tibial trials for knee anthroplasty
US9820868B2 (en) 2015-03-30 2017-11-21 Biomet Manufacturing, Llc Method and apparatus for a pin apparatus
US11801064B2 (en) 2015-06-25 2023-10-31 Biomet Manufacturing, Llc Patient-specific humeral guide designs
US10568647B2 (en) 2015-06-25 2020-02-25 Biomet Manufacturing, Llc Patient-specific humeral guide designs
US10925622B2 (en) 2015-06-25 2021-02-23 Biomet Manufacturing, Llc Patient-specific humeral guide designs
US10226262B2 (en) 2015-06-25 2019-03-12 Biomet Manufacturing, Llc Patient-specific humeral guide designs
US10722310B2 (en) 2017-03-13 2020-07-28 Zimmer Biomet CMF and Thoracic, LLC Virtual surgery planning system and method
US11298747B2 (en) 2017-05-18 2022-04-12 Howmedica Osteonics Corp. High fatigue strength porous structure
US11684478B2 (en) 2017-05-18 2023-06-27 Howmedica Osteonics Corp. High fatigue strength porous structure
US10736748B2 (en) 2018-05-02 2020-08-11 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a hinged-knee prosthesis
US11833053B2 (en) 2018-05-02 2023-12-05 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a hinged-knee prosthesis
US11696834B2 (en) 2019-02-05 2023-07-11 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a rotating hinged-knee prosthesis
US11116641B2 (en) 2019-02-05 2021-09-14 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a rotating hinged-knee prosthesis
US11033396B2 (en) 2019-02-05 2021-06-15 Depuy Ireland Unlimited Company Orthopaedic prosthetic system for a rotating hinged-knee prosthesis
CN111297520A (en) * 2020-03-23 2020-06-19 北京市春立正达医疗器械股份有限公司 Biological type tibial plateau holds in palm and platform pad

Also Published As

Publication number Publication date
US20050192672A1 (en) 2005-09-01
DE60305115D1 (en) 2006-06-14
DE60305115T2 (en) 2006-11-30
AU2003244616B2 (en) 2008-08-21
EP1400220B1 (en) 2006-05-10
ATE325587T1 (en) 2006-06-15
AU2003244616A1 (en) 2004-04-01
US20130150976A1 (en) 2013-06-13
DK1400220T3 (en) 2006-08-28
US8382847B2 (en) 2013-02-26
EP1400220A1 (en) 2004-03-24
ES2263923T3 (en) 2006-12-16

Similar Documents

Publication Publication Date Title
US8382847B2 (en) Posterior stabilized knee with varus-valgus constraint
US11369477B2 (en) High performance knee prostheses
US8202323B2 (en) Knee prostheses with enhanced kinematics
US9265615B2 (en) Systems and methods for providing deeper knee flexion capabilities for knee prosthesis patients
JP4307162B2 (en) Modular knee prosthesis
US6206926B1 (en) Prosthetic knee joint with enhanced posterior stabilization and dislocation prevention features
EP1604623B1 (en) Posterior stabilized mobile bearing knee
US8337564B2 (en) Total knee replacement prosthesis
AU697225B2 (en) Joint prosthesis
US6764516B2 (en) Posterior stabilized knee replacement with bearing translation for knees with retained collateral ligaments
US5370701A (en) Rotating/sliding contrained prosthetic knee
AU2016210692B2 (en) Modular hinge knee prosthesis and improvements of same
EP0916321A2 (en) Prosthetic knee joint with enhanced posterior stabilization and dislocation prevention features

Legal Events

Date Code Title Description
AS Assignment

Owner name: DEPUY PRODUCTS, INC., INDIANA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:WYSS, JOE;VOSLER, MARC C.;DIETZ, TERRY;AND OTHERS;REEL/FRAME:013733/0142;SIGNING DATES FROM 20021205 TO 20030117

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION