BEUDAMED
    FDA PMA FDA Class 3 Approved (Withdrawn) 🇺🇸 United States

    Stimulator, Functional Neuromuscular, Scoliosis

    PMA: P820008 · Decision Jan 6, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Stimulator, Functional Neuromuscular, Scoliosis
    Trade Name
    SCOLITRON(TM) STIMULATOR
    PMA Number
    P820008
    Device Class
    FDA Class 3
    Product Code
    LWB
    Generic Name
    Stimulator, functional neuromuscular, scoliosis
    Medical Specialty
    Unknown
    Advisory Committee
    Physical Medicine
    Decision
    Approved (Withdrawn)
    Decision Code
    APWD
    Decision Date
    January 6, 1983
    Date Received
    January 29, 1982
    Expedited Review
    N
    Docket Number
    83M-0053

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LWB Stimulator, Functional Neuromuscular, Scoliosis