BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Permanent Pacemaker Electrode

    PMA: P930039 · Supplement: S006 · Decision Aug 12, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24

    Basic Information

    Device Name
    Permanent Pacemaker Electrode
    Trade Name
    SUREFIX TM MODEL 5072 LEAD
    PMA Number
    P930039
    Supplement Number
    S006
    Device Class
    FDA Class 3
    Product Code
    DTB
    Generic Name
    permanent pacemaker Electrode
    Regulation Number
    870.3680
    Medical Specialty
    Cardiovascular
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    August 12, 1998
    Date Received
    April 20, 1998
    Expedited Review
    N

    Advisory Committee Statement

    Approval for a manufacturing site lcoated at Medtronic Puerto Rico, Inc., (MPRI), Road 149, Rm. 56.3, Villalba, Puerto Rico 00755.

    Classifications

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

    Product Code Device Name
    DTB Permanent Pacemaker Electrode