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

    WHITESIDE ORTHOLOC TOTAL HIP FEMORAL

    K Number: K842559 · Decision Dec 20, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    147
    Registration Numbers
    147
    Same Product Code
    103
    Applicant Total
    31
    Review Days
    171

    Basic Information

    Device Name
    WHITESIDE ORTHOLOC TOTAL HIP FEMORAL
    K Number
    K842559
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3360
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    DOW CORNING CORP. HEALTHCARE INDUSTRIES MATERIALS
    Date Received
    July 2, 1984
    Decision Date
    December 20, 1984
    Product Code
    KWL
    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
    KWL Prosthesis, Hip, Hemi-, Femoral, Metal

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