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

    METS MODULAR PROXIMAL FEMUR

    K Number: K121056 · Decision Sep 20, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    227
    Registration Numbers
    227
    Same Product Code
    562
    Applicant Total
    8
    Review Days
    167

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    Basic Information

    Device Name
    METS MODULAR PROXIMAL FEMUR
    K Number
    K121056
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3350
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Stanmore Implants Worldwide , Ltd.
    Date Received
    April 6, 2012
    Decision Date
    September 20, 2012
    Product Code
    JDI
    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
    JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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    Other Clearances by Stanmore Implants Worldwide , Ltd.

    K Number Device Name
    K140898 PATIENT SPECIFIC DISTAL FEMORAL
    K133152 JTS EXTENDIBLE DISTAL FEMORAL IMPLANT
    K121765 SCULPTOR ROBOTIC GUIDANCE ARM (RGA)
    K121029 METS MODULAR DISTAL FEMUR
    K121055 METS MODULAR TOTAL FEMUR
    K120992 METS SMILES TOTAL KNEE REPLACEMENT
    K092138 JTS EXTENDEABLE IMPLANT