BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Autonomic Nerve, Implanted (Depression)

    PMA: P970003 · Supplement: S162 · Decision Jul 10, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1

    Basic Information

    Device Name
    Stimulator, Autonomic Nerve, Implanted (Depression)
    Trade Name
    VNS THERAPY GENERATOR (DEMIPULSE) (ASPIREHC)
    PMA Number
    P970003
    Supplement Number
    S162
    Device Class
    FDA Class 3
    Product Code
    MUZ
    Generic Name
    Stimulator, autonomic nerve, implanted (depression)
    Medical Specialty
    Unknown
    Advisory Committee
    Neurology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 10, 2013
    Date Received
    April 22, 2013
    Supplement Type
    Real-Time Process
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR A CHANGE TO THE TRANSMIT TO RECEIVE REFRACTORY TIMEWHICH IS A SPECIFICATION OF THE APPLICATION SPECIFIC INTEGRATED CIRCUIT (ASIC) USED IN MODEL 103/104/105 VNS GENERATORS AND THE IMPLEMENTATION OF A SCREENING TEST TO BE PERFORMED AT THEVENDOR (ON SEMICONDUCTOR).

    Classifications

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

    Product Code Device Name
    MUZ Stimulator, Autonomic Nerve, Implanted (Depression)