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

    ZIRCONIA 22.22MM CERAMIC MODULAR HEADS

    K Number: K991708 · Decision Jul 30, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    276
    Same Product Code
    530
    Applicant Total
    441
    Review Days
    72

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    Basic Information

    Device Name
    ZIRCONIA 22.22MM CERAMIC MODULAR HEADS
    K Number
    K991708
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    888.3353
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biomet, Inc.
    Date Received
    May 19, 1999
    Decision Date
    July 30, 1999
    Product Code
    LZO
    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
    LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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