BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Electrical, Implantable, For Incontinence

    PMA: P970004 · Supplement: S010 · Decision Jun 28, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    20
    Registration Numbers
    20

    Basic Information

    Device Name
    Stimulator, Electrical, Implantable, For Incontinence
    Trade Name
    INTERSTIM SACRAL NERVE STIMULATION SYSTEM
    PMA Number
    P970004
    Supplement Number
    S010
    Device Class
    FDA Class 3
    Product Code
    EZW
    Generic Name
    Stimulator, electrical, implantable, for incontinence
    Regulation Number
    876.5270
    Medical Specialty
    Gastroenterology, Urology
    Advisory Committee
    Gastroenterology, Urology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    June 28, 2000
    Date Received
    June 20, 2000
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR 1) INCLUSION OF DEPTH INDICATORS ALONG THE BODY OF THE MODEL 3057 TEST STIMULATION LEAD AND ASSOCIATED LABELING CHANGES (3057 TEST STIMULATION COMPONENTS MANUAL AND 3065U MANUAL), AND 2) OTHER MINOR LABELING CHANGES TO THESE MANUALS FOR CLARIFICATION OF INSTRUCTIONS AND MINOR REFINEMENTS TO THE LEAD TESTING SPECIFICATIONS.

    Classifications

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

    Product Code Device Name
    EZW Stimulator, Electrical, Implantable, For Incontinence