BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Device, Thermal Ablation, Endometrial

    PMA: P010013 · Supplement: S002 · Decision Jun 5, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    19
    Registration Numbers
    19

    Basic Information

    Device Name
    Device, Thermal Ablation, Endometrial
    Trade Name
    NOVASURE IMPEDANCE CONTROLLED ENDOMETRIAL ABLATION SYSTEM
    PMA Number
    P010013
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    MNB
    Generic Name
    Device, thermal ablation, endometrial
    Medical Specialty
    Unknown
    Advisory Committee
    Obstetrics/Gynecology
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    June 5, 2002
    Date Received
    May 8, 2002
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    MODIFICATIONS TO THE MANUFACTURING PROCESSES FOR THE NOVASURE DISPOSABLE DEVICE, INCLUDING INJECTION MOLDING OF THE PLASTIC COMPONENTS, INCORPORATION OF THE NON-CONDUCTING LINES OF THE ARRAY INTO THE PEAK II KNITTING PROCESS, AND THE INCORPORATION OF THREE SEPARATE TUBES INTO A SINGLE MULTI-LUMEN EXTRUSION.

    Classifications

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

    Product Code Device Name
    MNB Device, Thermal Ablation, Endometrial