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

    STRAIGHT STEM FEMORAL HEAD PROSTHESIS

    K Number: K831851 · Decision Oct 6, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    106
    Applicant Total
    1
    Review Days
    119

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    Basic Information

    Device Name
    STRAIGHT STEM FEMORAL HEAD PROSTHESIS
    K Number
    K831851
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3360
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Proteck, Inc.
    Date Received
    June 9, 1983
    Decision Date
    October 6, 1983
    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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