BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implantable Pulse Generator

    PMA: P180036 · Supplement: S031 · Decision Aug 30, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2

    Basic Information

    Device Name
    Implantable Pulse Generator
    Trade Name
    GUARDIO/VESTA Charger firmware
    PMA Number
    P180036
    Supplement Number
    S031
    Device Class
    FDA Class 3
    Product Code
    QFV
    Generic Name
    Implantable pulse generator
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    August 30, 2024
    Date Received
    June 5, 2024
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    approval for changes to the GUARDIO and VESTA charger firmware, including updates and improvements to routines used when communicating with the cellular network, and to include a new information screen

    Classifications

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

    Product Code Device Name
    QFV Implantable Pulse Generator