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

    POLYETHYLENE MEDULLARY PLUG

    K Number: K811060 · Decision May 1, 1981
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    14

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    Basic Information

    Device Name
    POLYETHYLENE MEDULLARY PLUG
    K Number
    K811060
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Arthur A. Checchi, Inc.
    Date Received
    April 17, 1981
    Decision Date
    May 1, 1981
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N