BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    TRABECULAR METAL TIBIAL AND FEMORAL CONE AUGMENTS

    K Number: K053340 · Decision Feb 27, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    219
    Registration Numbers
    219
    Same Product Code
    142
    Applicant Total
    10
    Review Days
    88

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    Basic Information

    Device Name
    TRABECULAR METAL TIBIAL AND FEMORAL CONE AUGMENTS
    K Number
    K053340
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3565
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Zimmer Trabecular
    Date Received
    December 1, 2005
    Decision Date
    February 27, 2006
    Product Code
    MBH
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

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    Other Clearances by Zimmer Trabecular

    K Number Device Name
    K061155 VISTA P VERTEBRAL BODY REPLACEMENT SYSTEM
    K061067 TRABECULAR METAL ACETABULAR AUGMENTS
    K052950 THE ZIMMER TMT TRABECULAR METAL VERTEBRAL BODY REPLACEMENT SYSTEM
    K051756 MODIFICATION TO:TRABECULAR METAL FEMORAL CONE AUGMENTS, MODELS 03-125-ZZZZ
    K050766 EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEM
    K050937 TRABECULAR METAL ACETABULAR REVISION SHELLS
    K050101 THE TRABECULAR METAL BONE STABILIZATION IMPLANT, MODEL 99-11197-XX-10
    K042871 TRABECULAR METAL ACETABULAR AUGMENTS, MODELS 4894-XXX-YY, 02-212-105XX3, 02-212-205XX3, 02-212-305XX3
    K043061 THE TRABECULAR METAL GLENOID - BIGLIANI/FLATOW THE COMPLETE SHOULDER SOLUTION, MODEL 4316-XX-XX