BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Neuromuscular, Implanted

    PMA: P950035 · Supplement: S002 · Decision Jul 28, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Stimulator, Neuromuscular, Implanted
    Trade Name
    NEUROCONTROL FREEHAND SYSTEM(R)
    PMA Number
    P950035
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    GZC
    Generic Name
    Stimulator, neuromuscular, implanted
    Regulation Number
    882.5860
    Medical Specialty
    Neurology
    Advisory Committee
    Ear, Nose, Throat
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 28, 1998
    Date Received
    June 29, 1998
    Supplement Type
    Special (Immediate Track)
    Supplement Reason
    Labeling Change - Indications/instructions/shelf life/tradename
    Expedited Review
    N

    Advisory Committee Statement

    Application submitted to inform the Agency of the potential for device malfunction induced by electrostatic discharge and the changes being implementing to address the effects of ESD on the device. The Special Supplement requested approval for revised manufacturing procedures, revised labeling for the clinician, and revised patient labeling.

    Classifications

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

    Product Code Device Name
    GZC Stimulator, Neuromuscular, Implanted