BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Cardiac Ablation Percutaneous Catheter

    PMA: P020045 · Supplement: S006 · Decision Oct 26, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    52
    Registration Numbers
    52

    Basic Information

    Device Name
    Cardiac Ablation Percutaneous Catheter
    Trade Name
    9F FREEZOR MAX SURGICAL CARDIAC CRYOABLATION DEVICE
    PMA Number
    P020045
    Supplement Number
    S006
    Device Class
    FDA Class 3
    Product Code
    LPB
    Generic Name
    Cardiac ablation percutaneous catheter
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    October 26, 2004
    Date Received
    May 10, 2004
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE 9F FREEZOR MAX SURGICAL CARDIAC CRYOABLATION DEVICE, A MODIFICATION TO THE FREEZOR XTRA CARDIAC CRYOABLATION SYSTEM PREVIOUSLY APPROVED UNDER P020045/S005. THE DEVICE IS INDICATED FOR MINIMALLY INVASIVE CARDIAC SURGERY PROCEDURES, INCLUDING SURGICAL TREATMENT OF CARDIAC ARRHYTHMIAS.

    Classifications

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

    Product Code Device Name
    LPB Cardiac Ablation Percutaneous Catheter