BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implantable Pacemaker Pulse-Generator

    PMA: P910020 · Supplement: S013 · Decision May 3, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28

    Basic Information

    Device Name
    Implantable Pacemaker Pulse-Generator
    Trade Name
    MARATHON FAMILY OF PULSE GENERATORS AND THE MODEL 531-66
    PMA Number
    P910020
    Supplement Number
    S013
    Device Class
    FDA Class 3
    Product Code
    DXY
    Generic Name
    implantable pacemaker Pulse-generator
    Regulation Number
    870.3610
    Medical Specialty
    Cardiovascular
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    May 3, 1996
    Date Received
    December 14, 1995
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE MARATHON FAMILY OF PULSE GENERATORS AND THE MODEL 531-66 GRAPHICS PROGRAM MODULE. THE MARATHON FAMILY OF PULSE GENERATORS CONSISTS OF THE FOLLOWING MODELS: - MARATHON DR MODELS 294-09, 293-09, 294-09R, 294-10; MARATHON SR MODELS 292-09, 291-09, 292-09R, 292-10, 292-09X; COSMOS 3 MODELS 283-09, 284-09, 284-09R

    Classifications

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

    Product Code Device Name
    DXY Implantable Pacemaker Pulse-Generator