BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Pulse Generator, Permanent, Implantable

    PMA: P890003 · Supplement: S120 · Decision Jun 7, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35

    Basic Information

    Device Name
    Pulse Generator, Permanent, Implantable
    Trade Name
    MEDTRONIC MODEL 2090 BURBOT AND SPLAKE PROGRAMMERS
    PMA Number
    P890003
    Supplement Number
    S120
    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
    June 7, 2007
    Date Received
    May 14, 2007
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR AN ALTERNATE HARD DISK DRIVE (HDD) USED ON MEDTRONIC MODEL 2090 ?BURBOT? THAT ALSO INCLUDES A MINOR DESIGN CHANGE AND AN ALTERNATE FLOPPY DISC DRIVE (FDD) USED ON BOTH MEDTRONIC MODEL 2090 ?SPLAKE? AND ?BURBOT? CARELINK PROGRAMMERS.

    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