BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    ARTHROSCOPE OPERATIVE KNIFE SET

    K Number: K771851 · Decision Oct 27, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    117
    Registration Numbers
    117
    Same Product Code
    8
    Applicant Total
    142
    Review Days
    28

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    Basic Information

    Device Name
    ARTHROSCOPE OPERATIVE KNIFE SET
    K Number
    K771851
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    888.4540
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Richard Wolf Medical Instruments Corp.
    Date Received
    September 29, 1977
    Decision Date
    October 27, 1977
    Product Code
    HTS
    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
    HTS Knife, Orthopedic

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