BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implantable Pulse Generator

    PMA: P180036 · Supplement: S012 · Decision Nov 14, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2

    Basic Information

    Device Name
    Implantable Pulse Generator
    Trade Name
    OPTIMIZER Smart Mini System
    PMA Number
    P180036
    Supplement Number
    S012
    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
    November 14, 2022
    Date Received
    December 23, 2021
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    Approval for the OPTIhome Remote Patient Monitoring System and Patient App for use as accessories to the OPTIMIZER Smart Mini System.

    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