WO2015089393A1 - Extended patellofemoral - Google Patents

Extended patellofemoral Download PDF

Info

Publication number
WO2015089393A1
WO2015089393A1 PCT/US2014/070005 US2014070005W WO2015089393A1 WO 2015089393 A1 WO2015089393 A1 WO 2015089393A1 US 2014070005 W US2014070005 W US 2014070005W WO 2015089393 A1 WO2015089393 A1 WO 2015089393A1
Authority
WO
WIPO (PCT)
Prior art keywords
femur
notch
patellofemoral
posterior
component
Prior art date
Application number
PCT/US2014/070005
Other languages
French (fr)
Inventor
Stuart L. Axelson, Jr.
Peter John Wellings
Michael C. Ferko
Original Assignee
Stryker Corporation
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 Stryker Corporation filed Critical Stryker Corporation
Priority to AU2014362195A priority Critical patent/AU2014362195B2/en
Priority to EP14870376.2A priority patent/EP3079634B1/en
Publication of WO2015089393A1 publication Critical patent/WO2015089393A1/en

Links

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
    • A61F2/3859Femoral components
    • 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
    • A61F2/3877Patellae or trochleae

Definitions

  • the present invention relates to patellofemoral implants and in particular relates to such implants having an extension portion designed to cover the medial and/or lateral aspect of the patellofemoral compartment posteriorly up to the intercondylar notch and condylopatellar notch.
  • the knee joint includes three bones, namely the femur, tibia and patella.
  • the distal end of the femur lies adjacent to the proximal end of the tibia while the patella lies adjacent the anterior portion of the femur.
  • the joint elements that engage one another are preferably covered by articular cartilage.
  • the distal end of the femur and the proximal end of the tibia are covered by articular cartilage, as is the posterior surface of the patella .
  • the articular cartilage of the knee joint may become damaged due to degeneration and/or wear, which may lead to bone-to-bone contact during articulation of the joint. This may result in significant pain and potential damage to the bone surfaces.
  • a knee replacement procedure may be required in cases where damage to the articular cartilage is significant.
  • the procedure may include at least partial replacement of one or bone of the knee joint. For instance, in a total knee replacement each of the bones of the knee joint is at least partially covered by implants.
  • a knee arthroplasty procedure may be limited to portions of one of the joints.
  • a patellofemoral procedure is limited to at least partial replacement of the engagement surfaces between the femur and the patella.
  • the medial and lateral condylopatellar notches represent a border between the patellofemoral and tibiofemoral articulations of the distal femur.
  • the condylopatellar notch is a concave depression formed between the patellofemoral compartment and the medial and lateral compartments respectively.
  • the concave depression is formed at least in part due to femoral contact with the tibial meniscus when the leg is extended.
  • the geometry of the concave depression is in contrast to the convex geometries of the adjacent compartments.
  • the sulcus of the condylopatellar notch forms a spline that represents a transition region or functional boarder between the compartments of the knee. This spline can be simplified to a best-fit line which substantially describes the location and trajectory of the border.
  • the patellofemoral implants of the present invention improve implant coverage of each compartment of the distal femur for a larger percentage of the population. By designing the implants to only cover the region inside the condylopatellar border, anatomical variability reduces and less implant sizes and shapes are required to cover more people. Extension of the lateral flange of the implants helps to ensure that the patella remains in contact with the implants instead of stepping off the implants when transitioning to native cartilage laterally of the distal femur, medial cartilage or a medial unicompartmental implant.
  • a first aspect of the present invention is a patellofemoral unicompartmental implant with a posterior periphery that extends posteriorly toward the medial and/or lateral condylopatellar notch without crossing the notch.
  • a patellofemoral implant may be used as a stand-alone device or in conjunction with a medial and/or lateral tibiofemoral unicompartmental implant each having an anterior periphery that extends anteriorly toward the respective medial and/or lateral condylopatellar notch without crossing the respective notch.
  • the patellofemoral implant preferably replaces the articular cartilage and bone in the patellofemoral compartment.
  • a lateral aspect of the implant is designed to cover a lateral aspect of the patellofemoral compartment posteriorly up to the condylopatellar notch and above the intercondylar notch without crossing the condylopatellar notch or contacting the intercondylar notch.
  • a second aspect of the present invention is a patellofemoral component for replacing at least a. portion of a femur comprising a lateral portion configured to cover at least a portion of the femur, an intermediate portion adjacent to t e lateral portion and configured to cover at least a portion of a length of a trochlear groove of the femur, and a medial portion adjacent to the intermediate portion and configured to cover at least a portion of the femur.
  • the patellofemoral components include an extension portion extending posteriorly from the intermediate portion towards an intercondvlar notch of the femur without contactina the intercondylar notch of the femur when the patellofemoral component is engaged to the femur.
  • extension portion extends posteriorly from the lateral portion and. the ⁇ nterinedi ate port ⁇ o .
  • the extension portion extends along at least a portion of a condylopatellar notch of the femur and substantially parallel to the condylopatellar notch without contacting the notch.
  • the medial portion covers at least a portion of an anterior portion of a medial condyle of the femur without contacting the condylopatellar notch and the extension portion covers at least a portion of a posterior portion of a lateral condyle of the femur without contacting the condylopatellar notch.
  • the lateral portion has a first posterior periphery
  • the intermediate portion has a second posterior periphery
  • the medial portion has a third posterior periphery
  • the extension portion is located at a junction between the first and second posterior peripheries.
  • the extension portion may protrude posteriorly from the junction as a nub portion.
  • the extention portion may protrude posteriorly from the junction along a substantial portion of the first posterior periphery.
  • a third aspect of the present invention is a knee replacement system for replacing at least a portion of a femur comprising a patellofemoral component including an extension portion extending posteriorly from a posterior periphery thereof towards an intercondylar notch of the femur without contacting the intercondylar notch of the femur when the patellofemoral component is engaged to the femur, and a condylar implant including a recessed portion opposed to the extension portion of the patellofemoral component when the condylar portion is engaged to a condyle of the femur, the recessed portion located adjacent the intercondylar notch of the femur without contacting the intercondylar notch.
  • the pa.tellofeinoral component includes a lateral portion configured to cover at least a portion of the femur.
  • the patellofemoral component includes an intermediate portion connected to the lateral portion configured, to cover at least a portion of a length of a trochlear groove of the femur.
  • the patellofemoral component further includes a medial portion connected to the intermediate portion configured to cover at least a portion of the femur .
  • the extension portion extends posteriorly from the intermediate portion towards a condylopatellar notch of the femur without contacting the notch .
  • the lateral portion has a first posterior periphery
  • the intermediate portion has a second posterior periphery
  • the medial portion has a third posterior periphery
  • the extension portion is located at a junction between the first and second posterior peripheries.
  • the extension portion may protrude posteriorly from the junction as a nub portion.
  • the extention portion may protrude posteriorly from the junction along a substantial portion of the first posterior periphery.
  • a fourth aspect of the present invention is a knee replacement system for replacing at leas a portion of a femur comprising a patellofemoral component including an extension portion configured to overlie a portion of a lateral condyle of the femur above an intercondylar notch of the femur without contacting the inte condylar notch of the femur when the patellofemoral implant is engaged to the femur, and a condylar implant including a recessed portion opposed to the extension portion of the patellofemoral component when the condylar portion is engaged to a condyle of the femur, the recessed portion located anteriorly to a condylopatellar notch of the femur
  • the extension portion extends posteriorly from a posterior periphery of the pa.tellofemorai component towards the condylopatellar notch of r.he femur without contacting the notch.
  • the pateliofemorai component includes a lateral portion having a first posterior periphery, an intermediate portion having a. second posterior periphery, a medial portion having a third, posterior periphery, and the extension portion is located at a junction between the first and. second posterior peripheries.
  • the extension portion may protrude posteriorly from the junction as a nub portion .
  • the ext.ent.ion portion may protrude posteriorly from the junction along a substantial portion of the first posterior periphery.
  • FIG. 1 is a topographic isometric view of a left femur.
  • FIG. 2 is a topographic distal view of a distal end of the left femur shown in FIG. 1.
  • FIG. 3A is topographic distal view of a traditional pateliofemorai implant engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 3B is a topographic distal view of the traditional pateliofemorai implant shown in FIG. 3 and a traditional lateral condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 3C is a topographic distal view of the traditional pateliofemorai implant shown in FIG. 3 and a traditional medial condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 4 is a topographic distal view of the traditional patellofemoral implant shown in FIG. 3A and traditional lateral and medial and condylar implants shown in FIGS. 3B and 3C respectively each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 5 is another topographic distal view of a distal end of a left femur showing the location of an intercondylar notch and a lateral condylopatellar notch line thereof.
  • FIG. 6 is another topographic distal view of a distal end of a left femur showing the location of an intercondylar notch and a medial condylopatellar notch line thereof .
  • FIG. 7A is an isometric view of one embodiment of a patellofemoral implant having a first-type extension portion.
  • FIG. 7B is a distal view of the patellofemoral implant of FIG. 7A.
  • FIG. 7C is a medial view of the patellofemoral implant of FIG. 7A.
  • FIG. 8A is an isometric view of one embodiment of a patellofemoral implant having a second-type extension portion.
  • FIG. 8B is a distal view of the patellofemoral implant of FIG. 8A.
  • FIG. 8C is a medial view of the patellofemoral implant of FIG. 8A.
  • FIG. 9A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 9B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 10A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C and one embodiment of a first-type truncated lateral condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 10B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C and one embodiment of a second-type truncated lateral condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 11A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C and one embodiment of a medial condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 11B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C and one embodiment of a medial condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 12A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C, the first-type truncated lateral condylar implant shown in FIG. 10A, and the medial condylar implant shown in FIGS. 11A-11B each engaged to the distal end of the left femur shown in FIG. 1.
  • FIG. 12B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C, the second-type truncated lateral condylar implant shown in FIG. 10B, and the medial condylar implant shown in FIGS. 11A-11B each engaged to the distal end of the left femur shown in FIG. 1.
  • FIGS. 1-2A are topographic isometric and distal views respectively of distal end 12 of femur 10 showing the contour of the outer surface thereof.
  • femur 10 is a left femur having three regions, namely the trochlear groove 14, lateral condyle 16, and medial condyle 18. The topography of these areas or regions is referenced generally by the varying line curvature thereof .
  • FIG. 3A is topographic distal view of a traditional patellofemoral implant 100 engaged to the distal end of the left femur shown in FIG. 1.
  • Implant 100 includes an articular surface 102 having an outer periphery 104 and a trochlear groove 106, for example.
  • the distal end 12 of femur 10 may be resected either by standard or custom instrumentation, including guides and reamers, for example.
  • articular surface 102 of implant 100 is generally located where the outer surface of the articular cartilage of the distal femur was located prior to any degeneration or wear thereof.
  • Surgeon preference however may be to alter the location of articular surface 102 of implant 100 once engaged to distal end 12 of femur 10 such that it is not located exactly where the outer surface of the articular cartilage of the distal femur was located prior to any degeneration of wear thereof .
  • Outer periphery 104 of implant 100 includes medial and lateral recesses 108, 110 located adjacent the medial and lateral aspect of the patellofemoral compartment and above or anterior to the condylopatellar notch line. These recesses 108, 110 provide adequate clearance for a traditional lateral condylar implant 120 and/or medial condylar implant 140 engaged to the distal end of the left femur as shown in FIGS. 3B and 3C.
  • Each of lateral and medial condylar implants 120, 140 include articular surfaces 122, 142 and outer peripheries 124, 144, respectively.
  • FIGS. 5 and 6 are other topographic distal views of a distal end of a left femur showing the location of an intercondylar notch 20 and lateral and medial condylopatellar notch lines 21, 27 respectively thereof. Intercondylar notch 20 and lateral and medial condylopatellar notch lines 21, 27 respectively thereof. Intercondylar notch 20 and lateral and medial condylopatellar notch lines 21, 27 respectively thereof. Intercondylar notch
  • a posterior distance Dl is defined as the distance between intercondylar notch 20 and intersection point 23 along sagittal plane 22.
  • An angle ⁇ 1 is the measurement of the acute internal/external rotational angle between condylopatellar notch line 21 and flexion axis 24 of the knee.
  • medial condylopatellar notch line 27 extends across medial condyle 18 and intersects sagittal plane 22 at intersection point 23.
  • a posterior distance D2 is defined as the distance between intercondylar notch 20 and intersection point 23 along sagittal plane 22.
  • An angle ⁇ 2 is the measurement of the acute internal/external rotational angle between condylopatellar notch line 27 and flexion axis 24 of the knee.
  • a morphological analysis of 921 computed tomography ("CT") scans shows that there is a 95% likelihood that lines 21, 27 representing the lateral and medial condylopatellar notch lines, respectively, lie in boundaries 25, 28, respectively as shown in the triangular shaded regions of FIGS. 5 and 6, respectively.
  • CT computed tomography
  • the mean posterior distance Dl is 6.4mm with a ⁇ 1.25mm variation as depicted by boundary 25.
  • the mean posterior distance D2 is 2.9mm with a ⁇ 1.20mm variation as depicted by boundary 28.
  • the mean angle ⁇ 1 is 22.7° with ⁇ 5.7° variation as depicted by boundary 25 and the mean angle ⁇ 2 is 47.1° with ⁇ 5.43° variation as depicted by boundary 28.
  • the morphological analysis described above is one method of characterizing the condylopatellar notch in one specified demographic.
  • the three dimensional curvature of the condylopatellar notch is simplified here as being represented as a line.
  • This analysis could be modified to represent the region as a series of arcs or a point field which may alter the shape and extents of the 95% likelihood region.
  • This analysis could also be modified to look at specific demographics such as genders, ethnicities, and sizing measures, for example, to design implants for those groups.
  • the analysis could be used to describe the notch over a large population to characterize a broad average shape. In any of these cases, the bounding region would then be used to define the extents of the implant extension/truncation to avoid crossing the notch.
  • the shape of the bounding region could also be used to shape the peripheries of the implant where it approaches the notch.
  • FIGS. 7A-7C show a first embodiment of a patellofemoral implant 200 having a first-type extension portion 260 and FIGS. 8A-8C show a second embodiment of a patellofemoral implant 300 having a second-type extension portion 360.
  • implant 200 includes a bone contacting surface 201, an articular surface 202 having an outer periphery 204 and a trochlear groove 206, for example.
  • Implant 200 further includes a first condylar portion 210 configured to cover at least a portion of lateral condyle 16 of femur 10, an intermediate portion 220 adjacent to first condylar portion 210 configured to cover at least a portion of a length of trochlear groove 14 of femur 10, and a second condylar portion 230 adjacent to intermediate portion 220 configured to cover at least a portion of medial condyle 18 of femur 10.
  • First condylar portion 210 has a first periphery 212
  • intermediate portion 220 has a second periphery 222
  • second condylar portion 230 has a third periphery 232.
  • Outer periphery 204 of implant 200 differs from outer periphery 104 of implant 100 in that outer periphery 204 of implant 200 includes an extension portion 260 having a first configuration projecting posteriorly from a posterior portion thereof.
  • Extension portion 260 is designed to cover at least a portion of a lateral aspect of the patellofemoral compartment posteriorly up to intercondylar notch 20 and condylopatellar notch line 21 of femur 10 when implant 200 is engaged to distal end 12 of femur 10 as shown in FIG. 9A.
  • Extension portion 260 has a substantially planar periphery and is located intermediate first and second peripheries 212, 222.
  • the periphery of extension portion 260 lies adjacent along a length of condylopatellar notch line 21 of femur 10 without crossing condylopatellar notch line 21.
  • the substantially planar periphery of extension portion 260 is substantially perpendicularly oriented to first periphery 212 of first condylar portion 210.
  • implant 300 includes a bone contacting surface 301, an articular surface 302 having an outer periphery 304 and a trochlear groove 306, for example.
  • Implant 300 further includes a first condylar portion 310 configured to cover at least a portion of lateral condyle 16 of femur 10, an intermediate portion 320 adjacent to first condylar portion 310 configured to cover at least a portion of a length of trochlear groove 14 of femur 10, and a second condylar portion 330 adjacent to intermediate portion 320 configured to cover at least a portion of medial condyle 18 of femur 10.
  • First condylar portion 310 has a first periphery 312, intermediate portion 320 has a second periphery 322 and second condylar portion 330 has a third periphery 332.
  • Outer periphery 304 of implant 300 differs from outer periphery 104 of implant 100 in that outer periphery 304 of implant 300 includes an extension portion 360 having a second configuration projecting posteriorly from a posterior portion thereof.
  • Extension portion 360 is designed to cover at least a portion of a lateral aspect of the patellofemoral compartment posteriorly up to intercondylar notch 20 and condylopatellar notch line 21 of femur 10 when implant 300 is engaged to distal end 12 of femur 10 as shown in FIG. 9B.
  • Extension portion 360 has a substantially planar periphery and is located intermediate first and second peripheries 312, 322.
  • the periphery of extension portion 360 lies most adjacent to condylopatellar notch line 21 of femur 10 at intermediate portion 320.
  • the substantially planar periphery of extension portion 360 is transverse to first periphery 312 of first condylar portion 310.
  • extension portions 260, 360 of patellofemoral implants 200, 300 allows more contact with the patella through active flexion than occurs with traditional patellofemoral implants such as implant 100 shown in FIG. 3, for example. Active flexion occurs at approximately 10-110 degrees between the tibial and femoral mechanical axes with deep flexion occurring beyond 110 degrees and up to approximately 150 degrees.
  • the geometry of extension portions 260, 360 of patellofemoral implants 200, 300, respectively also accounts for unicondylar implants with truncated geometry to accommodate patellofemoral implants 200, 300 and to stay out of contact with patella in active flexion. Such unicondylar implants 400, 500 with truncated geometry are shown in FIGS. 10A and 10B, respectively.
  • FIGS. 11A and 11B show patellofemoral implants 200, 300 and medial condylar implants 600, 700 respectively each engaged to distal end 12 of femur 10.
  • FIGS. 12A and 12B show patellofemoral implants 200, 300, truncated unicondylar implants 400, 500 and medial condylar implants 700 respectively each engaged to distal end 12 of femur 10.
  • Without extension portions 260, 360 on patellofemoral implants 200, 300 the patella will frequently transition off and on patellofemoral implants 200, 300 during active flexion increasing the likelihood of failure if implantation is not ideal and implant materials are not well matched.
  • a traditional patellofemoral implant such as implant 100 does not allow a lateral tibiofemoral implant such as implant 120 to be truncated without increasing the distance over which the patella must articulate with native cartilage, for example. While an extended lateral tibiofemoral component may be thought of as a solution to this problem, such an implant can be challenging to fit on many patients due to the relative variability of the peripheries of the patellofemoral and tibiofemoral compartments on either side of the condylopatellar notch 16 of a patient. Extended patellofemoral implants 200, 300 increases the length of contact with the patella during active flexion and indirectly decreases the variability of the periphery required to be covered in both the patellofemoral and tibiofemoral compartments.
  • extension portion or posterior lateral periphery 260, 360 of extended patellofemoral implants 200, 300, respectively, is therefore extended to lie adjacent to condylopatellar notch line 21 without crossing the condylopatellar notch line 21.
  • the anterior peripheries 460, 560 of the matched lateral tibiofemoral implants 400, 500, respectively, can then be truncated to remain posterior of the condylopatellar notch 16 as shown in FIGS. 10A and 10B.
  • this preferably reduces the likelihood of a patellar implant from coming in contact with native cartilage.
  • Decreased contact between native cartilage and patellar implant articular bearing materials reduces the likelihood of unfavorable material interactions with native cartilage.
  • the increased patellofemoral contact length would reduce the frequency and likelihood of patellar transition from the patellofemoral implant to the lateral tibiofemoral implant. The reduction in the number of transitions from implant to implant preferably aid in increasing the life of the implant.
  • the extended patellofemoral implants 200, 300 and their matched truncated lateral tibiofemoral implant 400, 500 can be implanted conventionally or using robotic surgical assistance.
  • Preoperative planning may be used as identification of the intercondylar notch and condylopatellar notch line and determining implant size and position relative to these locations may require computational analysis .
  • Conventional implantation could be similar to the Avon patellofemoral implant manufactured by Stryker Orthopaedics, for example.
  • Robotic implantation would consist of preoperative planning, machining of patellofemoral compartment, implantation, trial reduction and cementation (if necessary).
  • the posterior periphery of the extended patellofemoral implants 200, 300 may be an inlay preparation, flush with the native cartilage, for example.
  • the anterior periphery could be an onlay preparation, proud of the resected bone, for example.

Abstract

Disclosed herein are knee replacement systems for replacing the articular surface of a distal femur. The systems include one or more unicompartmental components, namely patellofemoral (200, 300), lateral condylar (400, 500) and medial condylar components (600, 700). The components are configured such that when engaged to the femur the peripheries thereof (212, 222, 312, 322, 332) do not cross specific locations and/or regions of the femur, namely the intercondylar notch (20) and condylopatellar notch lines (21, 27). The patellofemoral components described herein preferably have an extension portion (260, 360) extending posteriorly from a posterior periphery thereof towards an intercondylar notch of the femur without contacting the intercondylar notch of the femur when the patellofemoral component is engaged to the femur. The extension portion preferably extends posteriorly from a posterior periphery of the patellofemoral component towards the condylopatellar notch of the femur without contacting the notch.

Description

EXTENDED PATELLOFEMORAL
CROSS-REFERENCE TO RELATED APPLICATIONS
[ 0001 ] The present application is a continuation of U.S. Patent Application No. 14/104,693, filed December 12, 2013, the disclosure of which is hereby incorporated herein by reference .
FIELD OF THE INVENTION
[ 0002 ] The present invention relates to patellofemoral implants and in particular relates to such implants having an extension portion designed to cover the medial and/or lateral aspect of the patellofemoral compartment posteriorly up to the intercondylar notch and condylopatellar notch.
BACKGROUND OF THE INVENTION
[ 0003 ] The knee joint includes three bones, namely the femur, tibia and patella. The distal end of the femur lies adjacent to the proximal end of the tibia while the patella lies adjacent the anterior portion of the femur. The joint elements that engage one another are preferably covered by articular cartilage. Specifically, the distal end of the femur and the proximal end of the tibia are covered by articular cartilage, as is the posterior surface of the patella .
[ 0004 ] The articular cartilage of the knee joint may become damaged due to degeneration and/or wear, which may lead to bone-to-bone contact during articulation of the joint. This may result in significant pain and potential damage to the bone surfaces. A knee replacement procedure may be required in cases where damage to the articular cartilage is significant. Depending on the extent of the damage, the procedure may include at least partial replacement of one or bone of the knee joint. For instance, in a total knee replacement each of the bones of the knee joint is at least partially covered by implants. In other instances, a knee arthroplasty procedure may be limited to portions of one of the joints. For instance, a patellofemoral procedure is limited to at least partial replacement of the engagement surfaces between the femur and the patella.
[ 0005 ] The medial and lateral condylopatellar notches represent a border between the patellofemoral and tibiofemoral articulations of the distal femur. The condylopatellar notch is a concave depression formed between the patellofemoral compartment and the medial and lateral compartments respectively. The concave depression is formed at least in part due to femoral contact with the tibial meniscus when the leg is extended. The geometry of the concave depression is in contrast to the convex geometries of the adjacent compartments. The sulcus of the condylopatellar notch forms a spline that represents a transition region or functional boarder between the compartments of the knee. This spline can be simplified to a best-fit line which substantially describes the location and trajectory of the border.
[ 0006 ] Conventional patellofemoral implants typically cover the femoral trochlea only and generally require that a lateral tibiofemoral component, for example, extend past the condylopatellar notch into the patellofemoral compartment. In the case where no lateral tibiofemoral implant is implanted, a surgeon must carefully plan the transition between the patellofemoral implant and the native cartilage. In such cases, it is expected that the patella will frequently transition from the patellofemoral component to the native condylar cartilage during active and deep flexion.
BRIEF SUMMARY OF THE INVENTION
[ 0007 ] The patellofemoral implants of the present invention improve implant coverage of each compartment of the distal femur for a larger percentage of the population. By designing the implants to only cover the region inside the condylopatellar border, anatomical variability reduces and less implant sizes and shapes are required to cover more people. Extension of the lateral flange of the implants helps to ensure that the patella remains in contact with the implants instead of stepping off the implants when transitioning to native cartilage laterally of the distal femur, medial cartilage or a medial unicompartmental implant.
[ 0008 ] A first aspect of the present invention is a patellofemoral unicompartmental implant with a posterior periphery that extends posteriorly toward the medial and/or lateral condylopatellar notch without crossing the notch. Such a patellofemoral implant may be used as a stand-alone device or in conjunction with a medial and/or lateral tibiofemoral unicompartmental implant each having an anterior periphery that extends anteriorly toward the respective medial and/or lateral condylopatellar notch without crossing the respective notch.
[ 0009 ] One embodiment of this first aspect is that the patellofemoral implant preferably replaces the articular cartilage and bone in the patellofemoral compartment. A lateral aspect of the implant is designed to cover a lateral aspect of the patellofemoral compartment posteriorly up to the condylopatellar notch and above the intercondylar notch without crossing the condylopatellar notch or contacting the intercondylar notch.
[ 0010 ] A second aspect of the present invention is a patellofemoral component for replacing at least a. portion of a femur comprising a lateral portion configured to cover at least a portion of the femur, an intermediate portion adjacent to t e lateral portion and configured to cover at least a portion of a length of a trochlear groove of the femur, and a medial portion adjacent to the intermediate portion and configured to cover at least a portion of the femur. The patellofemoral components include an extension portion extending posteriorly from the intermediate portion towards an intercondvlar notch of the femur without contactina the intercondylar notch of the femur when the patellofemoral component is engaged to the femur.
[ 0011 ] In one embodiment of this second aspect the extension portion extends posteriorly from the lateral portion and. the ίnterinedi ate portίo .
[ 0012 ] In another embodiment, the extension portion extends along at least a portion of a condylopatellar notch of the femur and substantially parallel to the condylopatellar notch without contacting the notch.
[ 0013 ] In yet another embodiment, the medial portion covers at least a portion of an anterior portion of a medial condyle of the femur without contacting the condylopatellar notch and the extension portion covers at least a portion of a posterior portion of a lateral condyle of the femur without contacting the condylopatellar notch.
[ 0014 ] In still yet another embodiment, the lateral portion has a first posterior periphery, the intermediate portion has a second posterior periphery, the medial portion has a third posterior periphery, and the extension portion is located at a junction between the first and second posterior peripheries. The extension portion may protrude posteriorly from the junction as a nub portion. The extention portion may protrude posteriorly from the junction along a substantial portion of the first posterior periphery.
[ 0015 ] A third aspect of the present invention is a knee replacement system for replacing at least a portion of a femur comprising a patellofemoral component including an extension portion extending posteriorly from a posterior periphery thereof towards an intercondylar notch of the femur without contacting the intercondylar notch of the femur when the patellofemoral component is engaged to the femur, and a condylar implant including a recessed portion opposed to the extension portion of the patellofemoral component when the condylar portion is engaged to a condyle of the femur, the recessed portion located adjacent the intercondylar notch of the femur without contacting the intercondylar notch.
[ 0016 ] In one embodiment of this third. aspect, the pa.tellofeinoral component includes a lateral portion configured to cover at least a portion of the femur.
[ 0017 ] In another embodiment, the patellofemoral component includes an intermediate portion connected to the lateral portion configured, to cover at least a portion of a length of a trochlear groove of the femur. The patellofemoral component further includes a medial portion connected to the intermediate portion configured to cover at least a portion of the femur .
[ 0018 ] In yet another embodiment, the extension portion extends posteriorly from the intermediate portion towards a condylopatellar notch of the femur without contacting the notch .
[ 0019 ] In still yet another embodiment, the lateral portion has a first posterior periphery, the intermediate portion has a second posterior periphery, the medial portion has a third posterior periphery, and the extension portion is located at a junction between the first and second posterior peripheries. The extension portion may protrude posteriorly from the junction as a nub portion. The extention portion may protrude posteriorly from the junction along a substantial portion of the first posterior periphery.
[ 0020 ] A fourth aspect of the present invention is a knee replacement system for replacing at leas a portion of a femur comprising a patellofemoral component including an extension portion configured to overlie a portion of a lateral condyle of the femur above an intercondylar notch of the femur without contacting the inte condylar notch of the femur when the patellofemoral implant is engaged to the femur, and a condylar implant including a recessed portion opposed to the extension portion of the patellofemoral component when the condylar portion is engaged to a condyle of the femur, the recessed portion located anteriorly to a condylopatellar notch of the femur„
[0021] In one embodiment of this aspect, the extension portion extends posteriorly from a posterior periphery of the pa.tellofemorai component towards the condylopatellar notch of r.he femur without contacting the notch.
[0022] In another embodiment, the pateliofemorai component includes a lateral portion having a first posterior periphery, an intermediate portion having a. second posterior periphery, a medial portion having a third, posterior periphery, and the extension portion is located at a junction between the first and. second posterior peripheries. The extension portion may protrude posteriorly from the junction as a nub portion . The ext.ent.ion portion may protrude posteriorly from the junction along a substantial portion of the first posterior periphery. BRIEF DESCRIPTION OF THE DRAWINGS
[0023] A more complete appreciation of the subject matter of the present invention and the various advantages thereof can be realized by reference to the following detailed description in which reference is made to the accompanying drawings in which :
[0024] FIG. 1 is a topographic isometric view of a left femur.
[0025] FIG. 2 is a topographic distal view of a distal end of the left femur shown in FIG. 1.
[0026] FIG. 3A is topographic distal view of a traditional pateliofemorai implant engaged to the distal end of the left femur shown in FIG. 1.
[0027] FIG. 3B is a topographic distal view of the traditional pateliofemorai implant shown in FIG. 3 and a traditional lateral condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
[0028] FIG. 3C is a topographic distal view of the traditional pateliofemorai implant shown in FIG. 3 and a traditional medial condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
[0029] FIG. 4 is a topographic distal view of the traditional patellofemoral implant shown in FIG. 3A and traditional lateral and medial and condylar implants shown in FIGS. 3B and 3C respectively each engaged to the distal end of the left femur shown in FIG. 1.
[0030] FIG. 5 is another topographic distal view of a distal end of a left femur showing the location of an intercondylar notch and a lateral condylopatellar notch line thereof.
[0031] FIG. 6 is another topographic distal view of a distal end of a left femur showing the location of an intercondylar notch and a medial condylopatellar notch line thereof .
[0032] FIG. 7A is an isometric view of one embodiment of a patellofemoral implant having a first-type extension portion.
[0033] FIG. 7B is a distal view of the patellofemoral implant of FIG. 7A.
[0034] FIG. 7C is a medial view of the patellofemoral implant of FIG. 7A.
[0035] FIG. 8A is an isometric view of one embodiment of a patellofemoral implant having a second-type extension portion.
[0036] FIG. 8B is a distal view of the patellofemoral implant of FIG. 8A.
[0037] FIG. 8C is a medial view of the patellofemoral implant of FIG. 8A.
[0038] FIG. 9A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C each engaged to the distal end of the left femur shown in FIG. 1.
[0039] FIG. 9B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C each engaged to the distal end of the left femur shown in FIG. 1.
[0040] FIG. 10A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C and one embodiment of a first-type truncated lateral condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
[ 0041 ] FIG. 10B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C and one embodiment of a second-type truncated lateral condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
[ 0042 ] FIG. 11A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C and one embodiment of a medial condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
[ 0043 ] FIG. 11B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C and one embodiment of a medial condylar implant each engaged to the distal end of the left femur shown in FIG. 1.
[ 0044 ] FIG. 12A is a topographic distal view of the patellofemoral implant shown in FIGS. 7A-7C, the first-type truncated lateral condylar implant shown in FIG. 10A, and the medial condylar implant shown in FIGS. 11A-11B each engaged to the distal end of the left femur shown in FIG. 1.
[ 0045 ] FIG. 12B is a topographic distal view of the patellofemoral implant shown in FIGS. 8A-8C, the second-type truncated lateral condylar implant shown in FIG. 10B, and the medial condylar implant shown in FIGS. 11A-11B each engaged to the distal end of the left femur shown in FIG. 1.
DETAILED DESCRIPTION
[ 0046 ] Referring to the drawings, wherein like reference numerals represent like elements, there is shown in the figures, in accordance with embodiments of the present invention, patellofemoral and condylar implants engaged to a resected distal end 12 of a femur, designated generally by reference numeral 10. FIGS. 1-2A are topographic isometric and distal views respectively of distal end 12 of femur 10 showing the contour of the outer surface thereof. As can be seen from these figures, femur 10 is a left femur having three regions, namely the trochlear groove 14, lateral condyle 16, and medial condyle 18. The topography of these areas or regions is referenced generally by the varying line curvature thereof .
[0047] FIG. 3A is topographic distal view of a traditional patellofemoral implant 100 engaged to the distal end of the left femur shown in FIG. 1. Implant 100 includes an articular surface 102 having an outer periphery 104 and a trochlear groove 106, for example. Prior to being engaged to the distal end 12 of the left femur 10 shown in FIG. 1, the distal end 12 of femur 10 may be resected either by standard or custom instrumentation, including guides and reamers, for example. Once engaged to distal end 12 of femur 10, articular surface 102 of implant 100 is generally located where the outer surface of the articular cartilage of the distal femur was located prior to any degeneration or wear thereof. Surgeon preference however may be to alter the location of articular surface 102 of implant 100 once engaged to distal end 12 of femur 10 such that it is not located exactly where the outer surface of the articular cartilage of the distal femur was located prior to any degeneration of wear thereof .
[0048] Outer periphery 104 of implant 100 includes medial and lateral recesses 108, 110 located adjacent the medial and lateral aspect of the patellofemoral compartment and above or anterior to the condylopatellar notch line. These recesses 108, 110 provide adequate clearance for a traditional lateral condylar implant 120 and/or medial condylar implant 140 engaged to the distal end of the left femur as shown in FIGS. 3B and 3C. Each of lateral and medial condylar implants 120, 140 include articular surfaces 122, 142 and outer peripheries 124, 144, respectively. An anterior portion 126, 146 of lateral and medial condylar implants 120, 140, respectively, lie substantially adjacent to recesses 110, 108 of implant 100 respectively, as shown in FIG. 6, for example. [0049] FIGS. 5 and 6 are other topographic distal views of a distal end of a left femur showing the location of an intercondylar notch 20 and lateral and medial condylopatellar notch lines 21, 27 respectively thereof. Intercondylar notch
20 is referenced as a point located in trochlear groove region 14.
[0050] As shown in FIG. 5, lateral condylopatellar notch line
21 extends across lateral condyle 16 and intersects sagittal plane 22 at intersection point 23. A posterior distance Dl is defined as the distance between intercondylar notch 20 and intersection point 23 along sagittal plane 22. An angle Θ1 is the measurement of the acute internal/external rotational angle between condylopatellar notch line 21 and flexion axis 24 of the knee.
[0051] As shown in FIG. 6, medial condylopatellar notch line 27 extends across medial condyle 18 and intersects sagittal plane 22 at intersection point 23. A posterior distance D2 is defined as the distance between intercondylar notch 20 and intersection point 23 along sagittal plane 22. An angle Θ2 is the measurement of the acute internal/external rotational angle between condylopatellar notch line 27 and flexion axis 24 of the knee.
[0052] A morphological analysis of 921 computed tomography ("CT") scans shows that there is a 95% likelihood that lines 21, 27 representing the lateral and medial condylopatellar notch lines, respectively, lie in boundaries 25, 28, respectively as shown in the triangular shaded regions of FIGS. 5 and 6, respectively. According to the morphological analysis, the mean posterior distance Dl is 6.4mm with a ±1.25mm variation as depicted by boundary 25. The mean posterior distance D2 is 2.9mm with a ±1.20mm variation as depicted by boundary 28. Further to the analysis, the mean angle Θ1 is 22.7° with ±5.7° variation as depicted by boundary 25 and the mean angle Θ2 is 47.1° with ±5.43° variation as depicted by boundary 28.
[ 0053 ] The morphological analysis described above is one method of characterizing the condylopatellar notch in one specified demographic. The three dimensional curvature of the condylopatellar notch is simplified here as being represented as a line. This analysis could be modified to represent the region as a series of arcs or a point field which may alter the shape and extents of the 95% likelihood region. This analysis could also be modified to look at specific demographics such as genders, ethnicities, and sizing measures, for example, to design implants for those groups. The analysis could be used to describe the notch over a large population to characterize a broad average shape. In any of these cases, the bounding region would then be used to define the extents of the implant extension/truncation to avoid crossing the notch. The shape of the bounding region could also be used to shape the peripheries of the implant where it approaches the notch.
[ 0054 ] FIGS. 7A-7C show a first embodiment of a patellofemoral implant 200 having a first-type extension portion 260 and FIGS. 8A-8C show a second embodiment of a patellofemoral implant 300 having a second-type extension portion 360.
[ 0055 ] As shown in FIGS. 7A-7C, implant 200 includes a bone contacting surface 201, an articular surface 202 having an outer periphery 204 and a trochlear groove 206, for example. Implant 200 further includes a first condylar portion 210 configured to cover at least a portion of lateral condyle 16 of femur 10, an intermediate portion 220 adjacent to first condylar portion 210 configured to cover at least a portion of a length of trochlear groove 14 of femur 10, and a second condylar portion 230 adjacent to intermediate portion 220 configured to cover at least a portion of medial condyle 18 of femur 10. First condylar portion 210 has a first periphery 212, intermediate portion 220 has a second periphery 222 and second condylar portion 230 has a third periphery 232.
[0056] Outer periphery 204 of implant 200 differs from outer periphery 104 of implant 100 in that outer periphery 204 of implant 200 includes an extension portion 260 having a first configuration projecting posteriorly from a posterior portion thereof. Extension portion 260 is designed to cover at least a portion of a lateral aspect of the patellofemoral compartment posteriorly up to intercondylar notch 20 and condylopatellar notch line 21 of femur 10 when implant 200 is engaged to distal end 12 of femur 10 as shown in FIG. 9A. Extension portion 260 has a substantially planar periphery and is located intermediate first and second peripheries 212, 222. The periphery of extension portion 260 lies adjacent along a length of condylopatellar notch line 21 of femur 10 without crossing condylopatellar notch line 21. In this embodiment, the substantially planar periphery of extension portion 260 is substantially perpendicularly oriented to first periphery 212 of first condylar portion 210.
[0057] As shown in FIGS. 8A-8C, implant 300 includes a bone contacting surface 301, an articular surface 302 having an outer periphery 304 and a trochlear groove 306, for example. Implant 300 further includes a first condylar portion 310 configured to cover at least a portion of lateral condyle 16 of femur 10, an intermediate portion 320 adjacent to first condylar portion 310 configured to cover at least a portion of a length of trochlear groove 14 of femur 10, and a second condylar portion 330 adjacent to intermediate portion 320 configured to cover at least a portion of medial condyle 18 of femur 10. First condylar portion 310 has a first periphery 312, intermediate portion 320 has a second periphery 322 and second condylar portion 330 has a third periphery 332.
[0058] Outer periphery 304 of implant 300 differs from outer periphery 104 of implant 100 in that outer periphery 304 of implant 300 includes an extension portion 360 having a second configuration projecting posteriorly from a posterior portion thereof. Extension portion 360 is designed to cover at least a portion of a lateral aspect of the patellofemoral compartment posteriorly up to intercondylar notch 20 and condylopatellar notch line 21 of femur 10 when implant 300 is engaged to distal end 12 of femur 10 as shown in FIG. 9B. Extension portion 360 has a substantially planar periphery and is located intermediate first and second peripheries 312, 322. The periphery of extension portion 360 lies most adjacent to condylopatellar notch line 21 of femur 10 at intermediate portion 320. In this embodiment, the substantially planar periphery of extension portion 360 is transverse to first periphery 312 of first condylar portion 310.
[0059] The geometry of extension portions 260, 360 of patellofemoral implants 200, 300, respectively, allows more contact with the patella through active flexion than occurs with traditional patellofemoral implants such as implant 100 shown in FIG. 3, for example. Active flexion occurs at approximately 10-110 degrees between the tibial and femoral mechanical axes with deep flexion occurring beyond 110 degrees and up to approximately 150 degrees. The geometry of extension portions 260, 360 of patellofemoral implants 200, 300, respectively, also accounts for unicondylar implants with truncated geometry to accommodate patellofemoral implants 200, 300 and to stay out of contact with patella in active flexion. Such unicondylar implants 400, 500 with truncated geometry are shown in FIGS. 10A and 10B, respectively.
[0060] FIGS. 11A and 11B show patellofemoral implants 200, 300 and medial condylar implants 600, 700 respectively each engaged to distal end 12 of femur 10. FIGS. 12A and 12B show patellofemoral implants 200, 300, truncated unicondylar implants 400, 500 and medial condylar implants 700 respectively each engaged to distal end 12 of femur 10. [ 0061 ] Without extension portions 260, 360 on patellofemoral implants 200, 300 the patella will frequently transition off and on patellofemoral implants 200, 300 during active flexion increasing the likelihood of failure if implantation is not ideal and implant materials are not well matched. A traditional patellofemoral implant such as implant 100 does not allow a lateral tibiofemoral implant such as implant 120 to be truncated without increasing the distance over which the patella must articulate with native cartilage, for example. While an extended lateral tibiofemoral component may be thought of as a solution to this problem, such an implant can be challenging to fit on many patients due to the relative variability of the peripheries of the patellofemoral and tibiofemoral compartments on either side of the condylopatellar notch 16 of a patient. Extended patellofemoral implants 200, 300 increases the length of contact with the patella during active flexion and indirectly decreases the variability of the periphery required to be covered in both the patellofemoral and tibiofemoral compartments.
[ 0062 ] The extension portion or posterior lateral periphery 260, 360 of extended patellofemoral implants 200, 300, respectively, is therefore extended to lie adjacent to condylopatellar notch line 21 without crossing the condylopatellar notch line 21. The anterior peripheries 460, 560 of the matched lateral tibiofemoral implants 400, 500, respectively, can then be truncated to remain posterior of the condylopatellar notch 16 as shown in FIGS. 10A and 10B.
[ 0063 ] Extending the posterior lateral periphery 260, 360 of patellofemoral implants 200, 300, respectively towards condylopatellar notch line 21 allows for a number of advantages. The extended articular surfaces allow a patellar implant to remain in contact with the patellofemoral implant for a greater range of active knee flexion. This increased contact length reduces the likelihood and frequency of patella transition off the patellofemoral implant.
[0064] In a medial and patellofemoral bicompartmental knee arthroplasty case, for example, this preferably reduces the likelihood of a patellar implant from coming in contact with native cartilage. Decreased contact between native cartilage and patellar implant articular bearing materials reduces the likelihood of unfavorable material interactions with native cartilage. In a tricompartmental case or a lateral and patellofemoral bicompartmental case, for example, the increased patellofemoral contact length would reduce the frequency and likelihood of patellar transition from the patellofemoral implant to the lateral tibiofemoral implant. The reduction in the number of transitions from implant to implant preferably aid in increasing the life of the implant.
[0065] By keeping the patellofemoral implant and lateral tibiofemoral implant on either side of the condylopatellar notch line, the potential variability of the implant periphery relative to patient's periphery is reduced. When either periphery of the patellofemoral or later tibiofemoral implant is required to cross this border on a patient, that implant is required to cover the periphery of its own compartment as well as the periphery of the adjacent compartment.
[0066] It is assumed that the relative positions of these compartments are uncorrelated as they were forged by their respective articular pair . With uncorrelated relative compartment positions, the periphery across the border can be assumed to be highly variable from patient to patient. Therefore the extension of the patellofemoral implant and truncation of the lateral tibiofemoral implant allow for a reduction in the variability of the patient peripheries they are required to cover .
[0067] The extended patellofemoral implants 200, 300 and their matched truncated lateral tibiofemoral implant 400, 500 can be implanted conventionally or using robotic surgical assistance. Preoperative planning may be used as identification of the intercondylar notch and condylopatellar notch line and determining implant size and position relative to these locations may require computational analysis . Conventional implantation could be similar to the Avon patellofemoral implant manufactured by Stryker Orthopaedics, for example. Robotic implantation would consist of preoperative planning, machining of patellofemoral compartment, implantation, trial reduction and cementation (if necessary). The posterior periphery of the extended patellofemoral implants 200, 300 may be an inlay preparation, flush with the native cartilage, for example. The anterior periphery could be an onlay preparation, proud of the resected bone, for example.
[ 0068 ] Although the invention herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present invention. It is therefore to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the present invention as defined by the appended claims .

Claims

1. A patellofemoral component for replacing at least a portion of a femur comprising:
a lateral portion configured to cover at least a lateral portion of the femur;
an intermediate portion adjacent to the lateral portion and configured to cover at least a portion of a length of a trochlear groove of the femur;
a medial portion adjacent to the intermediate portion and configured, to cover at least a medial portion of the femur; and
an extension portion extending posteriorly from the intermediate portion towards an intercondylar notch of the femur without contacting the intercondylar notch of the femur when the patellof moral component is engaged to the femur.
2. The patellofemoral component of claim 1, wherein the extension portion extends posteriorly from the lateral portion and t e intermediate portion,
3. The patellofemoral component of claim 1, wherein the extension portion extends along at least a portion of a condylopatellar notch of the femur and substantially parallel to the condylopatellar notch without contacting the notch .
4. The patellofemoral component of claim 1, wherein the medial portion covers at least a portion of an anterior portion of a medial condyle of the femur without contacting the condylopatellar notch.
5. The patellofemoral component of claim lf wherein the extension portion covers at least a portion of a posterior portion of a laterai condyle of the femur without contacting the condylopatellar notch,
6. The pateiiofemoral component of claim 1, wherein the lateral portion has a first posterior periphery, the intermediate portion has a second posterior periphery, the medial portion has a third posterior periphery, and the extension portion is located at a junction between the first and second posterior peripheries,
7. The pateiiofemoral component of claim 6, wherein the extension portion protrudes posteriorly from the junction as a nub portion.
8. The pateiiofemoral component of claim 6, wherein the extension portion protrudes posteriorly from the junction along a substantial portion of the first posterior periphery ,
9. A knee replacement system for replacing at least a portion of a femur comprising- :
a pateiio emoral component including an extension portion extending posteriorly from a posterior periphery thereof towards an intercondylar notch of the femur without contacting the inte condylar notch of the femur when the pateiiofemoral component is engaged to the femur; and
a condylar implant including a recessed portion opposed to the extension portion of the pateiiofemoral component when the condylar portion is engaged to a condyle of the femur, the recessed portion located adjacent the inte condylar notch of the femur without contacting the intercondylar notch.
1G. The knee replacement system of claim 9, wherein the patellofemoral component includes a lateral portion configured to cover at least a lateral portion of the femur.
11. The knee replacement system of claim 10, wherein the patellofemoral component includes an intermediate portion connected to the lateral portion configured to cover at least a portion of a. lengt of a trochlear groove of the femur .
12. The knee replacement system of claim 11, wherein the patellofemoral component includes a. medial portion connected to the intermediate portion configured to cover at least a. medial portion of the femur.
13. The knee replacement system of claim .12, wherein the extension portion extends posteriorly from the intermediate portion towards a condylopatellar notch of the femur without contacting the notch.
14. The knee replacement system of claim 11, wherein the lateral portion has a first posterior periphery, the intermediate portion has a second posterior periphery, the medial portion has a third posterior periphery, and the extension portion is located at a junction between the first and second posterior peripheries.
15. The knee replacement system of claim 14, wherein the extension portion protrudes posteriorly from the junction as a nub portion.
16. The patellofemoral component of claim 14, wherei the extension portion protrudes posteriorly from the "junction along- a substantial portion of t", e first", posterior- pe iphery .
17. A knee replacement system for replacing at least a portion of a femur comprising:
a pateliofemoral component including an extension portion configured to overlie a portion of a lateral condyle of the femur above an inte condylar notch of the femur without contacting the intercondylar notch of the femur when the pateliofemoral implant is engaged to the femur; and
a condylar implant including a recessed portion opposed to the extension portion of the pateliofemoral component when the condylar portion is engaged to a condyle of the femur, the recessed portion located, anteriorly to a condylopatellar notch of the femur.
IS. The knee replacement system of claim 17, wherein the extension portion extends posteriorly from a posterior periphery of the pateliofemoral component towards the condylopatellar notch of the femur without contacting the notch .
19. The knee replacement system of claim 17, wherein the pateliofemoral component includes a lateral portion having a first posterior periphery, an intermediate portion having a second posterior periphery, a medial portion having a third posterior periphery, and the extension portion is located, at. a junction between the first and second posterior peripheries .
20. The knee replacement system of claim 19, wherein the extension portion protrudes posteriorly from the junction as a nub portion.
21. The patellofemoral component of claim 19, wherein the extension portion protrudes posteriorly from the junction along- a substantial portion of the first posterior pe iphery .
PCT/US2014/070005 2013-12-12 2014-12-12 Extended patellofemoral WO2015089393A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU2014362195A AU2014362195B2 (en) 2013-12-12 2014-12-12 Extended patellofemoral
EP14870376.2A EP3079634B1 (en) 2013-12-12 2014-12-12 Extended patellofemoral

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US14/104,693 US9655727B2 (en) 2013-12-12 2013-12-12 Extended patellofemoral
US14/104,693 2013-12-12

Publications (1)

Publication Number Publication Date
WO2015089393A1 true WO2015089393A1 (en) 2015-06-18

Family

ID=53367055

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2014/070005 WO2015089393A1 (en) 2013-12-12 2014-12-12 Extended patellofemoral

Country Status (4)

Country Link
US (2) US9655727B2 (en)
EP (1) EP3079634B1 (en)
AU (1) AU2014362195B2 (en)
WO (1) WO2015089393A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9730797B2 (en) * 2011-10-27 2017-08-15 Toby Orthopaedics, Inc. Bone joint replacement and repair assembly and method of repairing and replacing a bone joint
US9655727B2 (en) * 2013-12-12 2017-05-23 Stryker Corporation Extended patellofemoral
CN110709033B (en) * 2017-06-04 2022-05-31 斯蒂芬·埃格利 Modular knee prosthesis
US10918487B2 (en) * 2018-07-25 2021-02-16 Orthopedix, Inc. Prosthetic implant caps
US10925746B2 (en) * 2018-07-25 2021-02-23 Orthopedix, Inc. Patient specific carpal implant
US11607323B2 (en) 2018-10-15 2023-03-21 Howmedica Osteonics Corp. Patellofemoral trial extractor

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050143833A1 (en) * 2001-08-07 2005-06-30 Merchant Alan C. Patello-femoral joint arthroplasty
US20070100460A1 (en) 2005-10-27 2007-05-03 Rhodes James M Orthopaedic implant systems with anti-abrasion studs
US20070219639A1 (en) 2006-03-14 2007-09-20 Mako Surgical Corporation Prosthetic device and system and method for implanting prosthetic device
US7544209B2 (en) * 2004-01-12 2009-06-09 Lotke Paul A Patello-femoral prosthesis
US20090228111A1 (en) 2008-03-04 2009-09-10 Mako Surgical Corp. Multi-compartmental prosthetic device with patellar component transition
US20120089147A1 (en) * 2010-10-11 2012-04-12 Cardo Medical, Inc. Methods And Apparatus For Preparing a Patient's Femur For Patellofemoral Knee Arthroplasty
US20120330429A1 (en) 2011-06-23 2012-12-27 Stryker Corporation Prosthetic implant and method of implantation

Family Cites Families (146)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3715763A (en) * 1971-04-21 1973-02-13 W Link Artificial limb for the knee joint
US3774244A (en) * 1972-02-08 1973-11-27 Relief Ruptured And Crippled S Knee-joint prosthesis
US4470158A (en) * 1978-03-10 1984-09-11 Biomedical Engineering Corp. Joint endoprosthesis
US5035699A (en) 1990-01-09 1991-07-30 Dow Corning Wright Patella track cutter and guide
US5163949A (en) 1990-03-02 1992-11-17 Bonutti Peter M Fluid operated retractors
US5092895A (en) * 1990-05-30 1992-03-03 Albrektsson Bjoern Knee-joint prosthesis
US5269785A (en) 1990-06-28 1993-12-14 Bonutti Peter M Apparatus and method for tissue removal
US6464713B2 (en) 1990-06-28 2002-10-15 Peter M. Bonutti Body tissue fastening
US6503277B2 (en) 1991-08-12 2003-01-07 Peter M. Bonutti Method of transplanting human body tissue
US5176684A (en) 1992-02-20 1993-01-05 Dow Corning Wright Modular shaping and trial reduction guide for implantation of posterior-stabilized femoral prosthesis and method of using same
US6074425A (en) * 1994-01-14 2000-06-13 Biomedical Engineering Trust I Fixed bearing joint endoprosthesis
FR2719762B1 (en) 1994-05-13 1996-07-12 Smith & Nephew Richards France Trochlear implant for femoro-patellar prosthesis and its fitting instrumentation.
US5755803A (en) 1994-09-02 1998-05-26 Hudson Surgical Design Prosthetic implant
US5824098A (en) 1994-10-24 1998-10-20 Stein; Daniel Patello-femoral joint replacement device and method
US5682886A (en) 1995-12-26 1997-11-04 Musculographics Inc Computer-assisted surgical system
US5702467A (en) 1996-06-12 1997-12-30 Johnson & Johnson Professional, Inc. Patellar resurfacing component
DE19646891A1 (en) * 1996-11-13 1998-05-14 Kubein Meesenburg Dietmar Artificial joint, especially an endoprosthesis to replace natural joints
DE19647155C2 (en) * 1996-11-14 1998-11-19 Plus Endoprothetik Ag Implant
US8545569B2 (en) * 2001-05-25 2013-10-01 Conformis, Inc. Patient selectable knee arthroplasty devices
US7618451B2 (en) 2001-05-25 2009-11-17 Conformis, Inc. Patient selectable joint arthroplasty devices and surgical tools facilitating increased accuracy, speed and simplicity in performing total and partial joint arthroplasty
US8480754B2 (en) * 2001-05-25 2013-07-09 Conformis, Inc. Patient-adapted and improved articular implants, designs and related guide tools
US8882847B2 (en) 2001-05-25 2014-11-11 Conformis, Inc. Patient selectable knee joint arthroplasty devices
US8234097B2 (en) * 2001-05-25 2012-07-31 Conformis, Inc. Automated systems for manufacturing patient-specific orthopedic implants and instrumentation
US5880976A (en) 1997-02-21 1999-03-09 Carnegie Mellon University Apparatus and method for facilitating the implantation of artificial components in joints
US6205411B1 (en) 1997-02-21 2001-03-20 Carnegie Mellon University Computer-assisted surgery planner and intra-operative guidance system
US6086593A (en) 1998-06-30 2000-07-11 Bonutti; Peter M. Method and apparatus for use in operating on a bone
US6099531A (en) 1998-08-20 2000-08-08 Bonutti; Peter M. Changing relationship between bones
US6616696B1 (en) * 1998-09-04 2003-09-09 Alan C. Merchant Modular knee replacement system
US6132468A (en) * 1998-09-10 2000-10-17 Mansmann; Kevin A. Arthroscopic replacement of cartilage using flexible inflatable envelopes
US7635390B1 (en) 2000-01-14 2009-12-22 Marctec, Llc Joint replacement component having a modular articulating surface
US6635073B2 (en) 2000-05-03 2003-10-21 Peter M. Bonutti Method of securing body tissue
US6702821B2 (en) 2000-01-14 2004-03-09 The Bonutti 2003 Trust A Instrumentation for minimally invasive joint replacement and methods for using same
US7104996B2 (en) 2000-01-14 2006-09-12 Marctec. Llc Method of performing surgery
US6770078B2 (en) 2000-01-14 2004-08-03 Peter M. Bonutti Movable knee implant and methods therefor
US6712856B1 (en) 2000-03-17 2004-03-30 Kinamed, Inc. Custom replacement device for resurfacing a femur and method of making the same
EP2314257B9 (en) 2000-05-01 2013-02-27 ArthroSurface, Inc. System for joint resurface repair
US8177841B2 (en) 2000-05-01 2012-05-15 Arthrosurface Inc. System and method for joint resurface repair
US7618462B2 (en) 2000-05-01 2009-11-17 Arthrosurface Incorporated System and method for joint resurface repair
US6610067B2 (en) 2000-05-01 2003-08-26 Arthrosurface, Incorporated System and method for joint resurface repair
US7678151B2 (en) 2000-05-01 2010-03-16 Ek Steven W System and method for joint resurface repair
US7713305B2 (en) 2000-05-01 2010-05-11 Arthrosurface, Inc. Articular surface implant
US20040230315A1 (en) 2000-05-01 2004-11-18 Ek Steven W. Articular surface implant
US7163541B2 (en) 2002-12-03 2007-01-16 Arthrosurface Incorporated Tibial resurfacing system
US6679917B2 (en) 2000-05-01 2004-01-20 Arthrosurface, Incorporated System and method for joint resurface repair
US6494914B2 (en) * 2000-12-05 2002-12-17 Biomet, Inc. Unicondylar femoral prosthesis and instruments
US6503280B2 (en) * 2000-12-26 2003-01-07 John A. Repicci Prosthetic knee and method of inserting
ATE353200T1 (en) * 2001-03-26 2007-02-15 Zimmer Gmbh KNEE PROSTHESIS
US6589283B1 (en) * 2001-05-15 2003-07-08 Biomet, Inc. Elongated femoral component
US20070173858A1 (en) 2001-06-14 2007-07-26 Alexandria Research Technologies, Llc Apparatus and Method for Sculpting the Surface of a Joint
US6723102B2 (en) 2001-06-14 2004-04-20 Alexandria Research Technologies, Llc Apparatus and method for minimally invasive total joint replacement
US6482209B1 (en) * 2001-06-14 2002-11-19 Gerard A. Engh Apparatus and method for sculpting the surface of a joint
US6364910B1 (en) 2001-07-11 2002-04-02 Biomet, Inc. Method and apparatus for use of a glenoid component
WO2003013339A2 (en) * 2001-08-07 2003-02-20 Depuy Orthopaedics, Inc. Patellar prosthetic arrangement and associated surgical method
US7559928B2 (en) 2002-02-12 2009-07-14 Alexandria Research Technologies, Llc Apparatus and method for minimally invasive total joint replacement
AU2003219773B2 (en) 2002-02-14 2007-02-01 Biomet Spain Orthopaedics S.L. Method and instrumentation for patello-femoral joint replacement
JP4193177B2 (en) * 2002-02-20 2008-12-10 ジンマー インコーポレーテッド Prosthesis and tibial implant device for knee arthroplasty
DE10220591B4 (en) * 2002-05-08 2004-03-18 Mathys Medizinaltechnik Ag Joint prosthesis with an intermediate element with different radii of curvature
US7150761B2 (en) * 2002-05-24 2006-12-19 Medicinelodge, Inc. Modular femoral components for knee arthroplasty
US20100185294A1 (en) 2002-06-04 2010-07-22 Arthrosurface Incorporated Nanorough Alloy Substrate
US20030225458A1 (en) 2002-06-04 2003-12-04 Ron Donkers Universal femoral component for endoprosthetic knee
US8211113B2 (en) 2002-06-21 2012-07-03 Depuy Products, Inc. Prosthesis cutting guide, cutting tool and method
AU2003287190A1 (en) * 2002-10-23 2004-05-13 Alastair J. T. Clemow Modular femoral component for a total knee joint replacement for minimally invasive implantation
US20040102852A1 (en) * 2002-11-22 2004-05-27 Johnson Erin M. Modular knee prosthesis
US6749638B1 (en) * 2002-11-22 2004-06-15 Zimmer Technology, Inc. Modular knee prosthesis
US7901408B2 (en) 2002-12-03 2011-03-08 Arthrosurface, Inc. System and method for retrograde procedure
US6800094B2 (en) 2003-01-21 2004-10-05 Zimmer Technology, Inc. Mobile bearing patellar prosthesis with orbital translation
US6916324B2 (en) * 2003-02-04 2005-07-12 Zimmer Technology, Inc. Provisional orthopedic prosthesis for partially resected bone
US20040153087A1 (en) * 2003-02-04 2004-08-05 Sanford Adam H. Provisional orthopedic implant with removable guide
US7172597B2 (en) * 2003-02-04 2007-02-06 Zimmer Technology, Inc. Provisional orthopedic implant and recutting instrument guide
DE10305591A1 (en) * 2003-02-05 2004-08-26 Aesculap Ag & Co. Kg implant
US6916341B2 (en) * 2003-02-20 2005-07-12 Lindsey R. Rolston Device and method for bicompartmental arthroplasty
US8388624B2 (en) 2003-02-24 2013-03-05 Arthrosurface Incorporated Trochlear resurfacing system and method
US7985225B2 (en) 2003-05-05 2011-07-26 Alexandria Research Technologies, Llc Apparatus and method for sculpting the surface of a joint
AU2003904379A0 (en) * 2003-08-18 2003-08-28 David John Wood Two thirds prosthetic arthroplasty
AU2006203909A1 (en) 2003-11-20 2006-07-13 Arthrosurface, Inc. System and method for retrograde procedure
US7951163B2 (en) 2003-11-20 2011-05-31 Arthrosurface, Inc. Retrograde excision system and apparatus
CA2546582A1 (en) 2003-11-20 2005-06-09 Arthrosurface, Inc. Retrograde delivery of resurfacing devices
US20050137708A1 (en) * 2003-12-23 2005-06-23 Ron Clark Device and method of arthroscopic knee joint resurfacing
EP1703867B1 (en) * 2004-01-12 2012-03-07 Depuy Products, Inc. Systems for compartmental replacement in a knee
US8002840B2 (en) * 2004-01-12 2011-08-23 Depuy Products, Inc. Systems and methods for compartmental replacement in a knee
US8535383B2 (en) * 2004-01-12 2013-09-17 DePuy Synthes Products, LLC Systems and methods for compartmental replacement in a knee
US20060030854A1 (en) 2004-02-02 2006-02-09 Haines Timothy G Methods and apparatus for wireplasty bone resection
US8114083B2 (en) 2004-01-14 2012-02-14 Hudson Surgical Design, Inc. Methods and apparatus for improved drilling and milling tools for resection
US7815645B2 (en) 2004-01-14 2010-10-19 Hudson Surgical Design, Inc. Methods and apparatus for pinplasty bone resection
US7857814B2 (en) 2004-01-14 2010-12-28 Hudson Surgical Design, Inc. Methods and apparatus for minimally invasive arthroplasty
US8021368B2 (en) 2004-01-14 2011-09-20 Hudson Surgical Design, Inc. Methods and apparatus for improved cutting tools for resection
AU2005200104B2 (en) * 2004-01-23 2009-12-17 Depuy Orthopaedics, Inc. Bone protector, kit and method
US20050165491A1 (en) * 2004-01-23 2005-07-28 Diaz Robert L. Method and apparatus for bi-compartmental partial knee replacement
US20060030855A1 (en) 2004-03-08 2006-02-09 Haines Timothy G Methods and apparatus for improved profile based resection
US20090270994A1 (en) * 2004-02-27 2009-10-29 Roberto Schaefer Medial and lateral femoral implants for single-compartment knee prosthesis
WO2006004885A2 (en) 2004-06-28 2006-01-12 Arthrosurface, Inc. System for articular surface replacement
US7806898B2 (en) 2004-07-09 2010-10-05 Zimmer, Inc. Modular guide systems and related rasps and methods for resecting a joint articulation surface
US8157867B2 (en) 2004-07-09 2012-04-17 Zimmer, Inc. Trochlear groove implants and related methods and instruments
CA2574290A1 (en) * 2004-07-20 2006-02-02 Alexandria Research Technologies, Llc Modular apparatus and method for sculpting the surface of a joint
US7828853B2 (en) 2004-11-22 2010-11-09 Arthrosurface, Inc. Articular surface implant and delivery system
US7581118B2 (en) 2004-12-14 2009-08-25 Netapp, Inc. Disk sanitization using encryption
US20060190086A1 (en) * 2005-02-22 2006-08-24 Mako Surgical Corporation Knee implant
US7578850B2 (en) * 2005-04-18 2009-08-25 Uni-Knee, Llc Unicondylar knee implant
US7695477B2 (en) 2005-05-26 2010-04-13 Zimmer, Inc. Milling system and methods for resecting a joint articulation surface
US8002777B2 (en) 2005-06-09 2011-08-23 Biomet Manufacturing Corp. Instrumentation and method for implanting a curved stem tibial tray
US8128631B2 (en) 2005-07-28 2012-03-06 Alexandria Research Technologies, Inc. Apparatus and method for placing an implant in vivo
CA2617217A1 (en) 2005-07-29 2007-02-08 Arthrosurface, Inc. System and method for articular surface repair
US7862619B2 (en) * 2005-08-05 2011-01-04 Vot, Llc Knee joint prosthesis
US20070043444A1 (en) * 2005-08-22 2007-02-22 Lester Don K Prosthetic device
US8216319B2 (en) * 2005-10-27 2012-07-10 Depuy Products, Inc. Method of repairing a knee joint
US8211181B2 (en) * 2005-12-14 2012-07-03 New York University Surface guided knee replacement
GB0526385D0 (en) * 2005-12-28 2006-02-08 Mcminn Derek J W Improvements in or relating to knee prosthesis
US8142509B2 (en) 2006-01-23 2012-03-27 Smith & Nephew, Inc. Patellar components
CA2645559C (en) * 2006-03-13 2016-04-12 Mako Surgical Corp. Prosthetic device and system and method for implanting prosthetic device
US20070270973A1 (en) 2006-04-10 2007-11-22 Alexandria Research Technologies, Llc Apparatus and method for sculpting the surface of a joint
US20070288021A1 (en) 2006-06-07 2007-12-13 Howmedica Osteonics Corp. Flexible joint implant
WO2008011409A2 (en) 2006-07-17 2008-01-24 Arthrosurface Incorporated System and method for tissue resection
CA2662785A1 (en) * 2006-09-06 2008-03-13 Smith & Nephew, Inc. Implants with transition surfaces and related processes
US20080119938A1 (en) * 2006-11-17 2008-05-22 Sang Soo Oh Knee joint prosthesis for bi-compartmental knee replacement and surgical devices thereof
US7896923B2 (en) * 2006-11-30 2011-03-01 Biomet Manufacturing Corp. Arthroscopic unicompartmental knee implantation system and related method
US9358029B2 (en) 2006-12-11 2016-06-07 Arthrosurface Incorporated Retrograde resection apparatus and method
US20080195221A1 (en) 2007-01-22 2008-08-14 Zimmer Gmbh Implant and a method for partial replacement of joint surfaces
US7582118B2 (en) * 2007-02-06 2009-09-01 Zimmer Technology, Inc. Femoral trochlea prostheses
US8128704B2 (en) * 2007-02-06 2012-03-06 Zimmer, Inc. Femoral trochlea prostheses
US20080195113A1 (en) 2007-02-14 2008-08-14 Arthrosurface Incorporated Bone Cement Delivery Device
MX2009010707A (en) 2007-04-04 2010-03-26 Alexandria Res Technologies Llc Apparatus and method for sculpting the surface of a joint.
US8265949B2 (en) 2007-09-27 2012-09-11 Depuy Products, Inc. Customized patient surgical plan
US20090132055A1 (en) * 2007-11-08 2009-05-21 Ferro Thomas D Arthroplasty device
US8361163B2 (en) 2007-12-10 2013-01-29 Mako Surgical Corp. Prosthetic device and system for preparing a bone to receive a prosthetic device
WO2009076293A2 (en) 2007-12-10 2009-06-18 Mako Surgical Corp. Prosthetic device and method for implanting the prosthetic device
US7896924B1 (en) * 2008-01-09 2011-03-01 Howmedica Osteonics Corp. Unicondylar femoral prosthetic implant component
AU2009212243B2 (en) * 2008-02-06 2014-08-07 Exactech, Inc. Femoral component of knee prosthesis, the femoral component having anterior/posterios claw(s) for digging into bone and/or a raised rib with a bulbous terminus
WO2009111481A1 (en) 2008-03-03 2009-09-11 Arthrosurface Incorporated Bone resurfacing system and method
GB0812631D0 (en) * 2008-07-10 2008-08-20 Imp Innovations Ltd Modular knee implants
CA2739269C (en) 2008-10-02 2017-03-14 Mako Surgical Corporation Prosthetic device for knee joint and methods of implanting and removing same
US8157868B2 (en) * 2008-10-10 2012-04-17 New York University Implants for the treatment of osteoarthritis of the knee
US9364291B2 (en) 2008-12-11 2016-06-14 Mako Surgical Corp. Implant planning using areas representing cartilage
USD625415S1 (en) 2008-12-19 2010-10-12 Mako Surgical Corp. Femoral implant
USD622854S1 (en) 2008-12-19 2010-08-31 Mako Surgical Corp. Patellofemoral implant
US20100217400A1 (en) 2009-02-24 2010-08-26 Mako Surgical Corp. Prosthetic device, method of planning bone removal for implantation of prosthetic device, and robotic system
WO2010121246A1 (en) 2009-04-17 2010-10-21 Arthrosurface Incorporated Glenoid resurfacing system and method
WO2010121250A1 (en) 2009-04-17 2010-10-21 Arthrosurface Incorporated Glenoid resurfacing system and method
US8945233B2 (en) 2009-07-10 2015-02-03 Peter Forsell Hip joint method
CA2792048A1 (en) 2010-03-05 2011-09-09 Arthrosurface Incorporated Tibial resurfacing system and method
US9271840B2 (en) 2010-03-10 2016-03-01 John Keggi Low stress all poly tibial component
EP2603173B1 (en) * 2010-08-12 2016-03-23 Smith & Nephew, Inc. Structures for use in orthopaedic implant fixation
US8702802B2 (en) * 2011-08-29 2014-04-22 Linares Medical Devices, Llc Knee implant assembly with rotary bearing supported and traveling surfaces
US8753403B2 (en) * 2011-08-30 2014-06-17 Linares Medical Devices, Llc Multi-component knee implant assembly with combined articulating and belt support and traveling surfaces
US20140142713A1 (en) * 2012-11-21 2014-05-22 Abraham P. Wright Knee prosthesis assembly having proportional trochlear groove geometry
US20140358241A1 (en) * 2013-06-04 2014-12-04 Jacques Afriat Total knee prosthesis, and set of modular elements making it possible to obtain such a prosthesis
US9655727B2 (en) * 2013-12-12 2017-05-23 Stryker Corporation Extended patellofemoral

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050143833A1 (en) * 2001-08-07 2005-06-30 Merchant Alan C. Patello-femoral joint arthroplasty
US7544209B2 (en) * 2004-01-12 2009-06-09 Lotke Paul A Patello-femoral prosthesis
US20070100460A1 (en) 2005-10-27 2007-05-03 Rhodes James M Orthopaedic implant systems with anti-abrasion studs
US20070219639A1 (en) 2006-03-14 2007-09-20 Mako Surgical Corporation Prosthetic device and system and method for implanting prosthetic device
US20090228111A1 (en) 2008-03-04 2009-09-10 Mako Surgical Corp. Multi-compartmental prosthetic device with patellar component transition
US20120089147A1 (en) * 2010-10-11 2012-04-12 Cardo Medical, Inc. Methods And Apparatus For Preparing a Patient's Femur For Patellofemoral Knee Arthroplasty
US20120330429A1 (en) 2011-06-23 2012-12-27 Stryker Corporation Prosthetic implant and method of implantation

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
VAN JONBERGEN, H. P. W. ET AL.: "Differences in the stress distribution in the distal femur between patellofemoral joint replacement and total knee replacement: a finite element study", JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH, vol. 7, no. 1, 2012, XP021107912 *

Also Published As

Publication number Publication date
US20170172749A1 (en) 2017-06-22
EP3079634A4 (en) 2017-07-26
AU2014362195A1 (en) 2016-06-23
EP3079634A1 (en) 2016-10-19
US10098747B2 (en) 2018-10-16
US9655727B2 (en) 2017-05-23
AU2014362195B2 (en) 2018-08-09
US20150164647A1 (en) 2015-06-18
EP3079634B1 (en) 2018-10-24

Similar Documents

Publication Publication Date Title
US10098747B2 (en) Extended patellofemoral
EP3348238B1 (en) Prosthetic knee implant
AU2018204902B2 (en) Constrained knee prosthesis
US9649195B2 (en) Femoral implant for preserving cruciate ligaments
AU2011300537B2 (en) Femoral extension prosthetic component and tibial shelf prosthetic component for unicondylar meniscal bearing knee prosthesis and prosthesis including such a component
EP2143403A1 (en) Knee Prosthesis
EP1684672A1 (en) High flexion articular insert
US9398958B2 (en) Knee prosthesis
US11331194B2 (en) Femoral component
AU2020235885A1 (en) Orthopaedic system with insert having a post for medial pivoting of a femoral component

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 14870376

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2014362195

Country of ref document: AU

Date of ref document: 20141212

Kind code of ref document: A

REEP Request for entry into the european phase

Ref document number: 2014870376

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2014870376

Country of ref document: EP