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

    APEX MODULAR ZIRCONIA FEMORAL HEAD

    K Number: K003923 · Decision Mar 20, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    276
    Same Product Code
    530
    Applicant Total
    6
    Review Days
    90

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    Basic Information

    Device Name
    APEX MODULAR ZIRCONIA FEMORAL HEAD
    K Number
    K003923
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3353
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Apex Surgical, LLC
    Date Received
    December 20, 2000
    Decision Date
    March 20, 2001
    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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    Other Clearances by Apex Surgical, LLC

    K Number Device Name
    K043123 APEX MODULAR HA HIP STEM
    K041950 APEX K2 HIP SYSTEM
    K031110 APEX MODULAR ACETABULAR CUP
    K012918 APEX MODULAR ALUMINA FEMORAL HEAD
    K000788 APEX MODULAR HIP STEM