BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Pulse Generator, Permanent, Implantable

    PMA: P980035 · Supplement: S140 · Decision Sep 25, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35

    Basic Information

    Device Name
    Pulse Generator, Permanent, Implantable
    Trade Name
    ADAPTA, VERSA, SENSIA AND RELIA IPG FAMILIES
    PMA Number
    P980035
    Supplement Number
    S140
    Device Class
    FDA Class 3
    Product Code
    NVZ
    Generic Name
    Pulse generator, permanent, implantable
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    September 25, 2009
    Date Received
    July 28, 2009
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR DESIGN CHANGES TO THE L368 INTEGRATED CIRCUIT INCLUDING MODIFICATIONS TO THE CHARGE AMP OFFSET CIRCUIT, AUTOPOLARITY SHORT CIRCUIT PACE THRESHOLD CIRCUIT, AND KEITHLEY STRUCTURE AS WELL AS A FAMILY IDENTIFICATION CHANGE IN THE INTEGRATED CIRCUIT FOR THE RELIA.

    Classifications

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

    Product Code Device Name
    NVZ Pulse Generator, Permanent, Implantable