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

    P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG

    K Number: K863854 · Decision Nov 19, 1986
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    48

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    Basic Information

    Device Name
    P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG
    K Number
    K863854
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Precision Medical Devices, Inc.
    Date Received
    October 2, 1986
    Decision Date
    November 19, 1986
    Advisory Committee
    Unknown
    Review Advisory Committee
    OR
    Third Party
    N

    Other Clearances by Precision Medical Devices, Inc.

    K Number Device Name
    K840856 MODULAR CONSTRUCT FRAME EXTERNAL FIXA
    K840046 PRESSURIZING/SCAVENGING ACRYLIC CEMENT