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

    CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5

    K Number: K953792 · Decision Nov 6, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    276
    Same Product Code
    530
    Applicant Total
    24
    Review Days
    84

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    Basic Information

    Device Name
    CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5
    K Number
    K953792
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3353
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    U.S. Medical Products, Inc.
    Date Received
    August 14, 1995
    Decision Date
    November 6, 1995
    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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