BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Low Electric Field, Tumor Treatment

    PMA: P100034 · Supplement: S002 · Decision Dec 3, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9

    Basic Information

    Device Name
    Stimulator, Low Electric Field, Tumor Treatment
    Trade Name
    NOVOTTF-100A SYSTEM
    PMA Number
    P100034
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    NZK
    Generic Name
    Stimulator, low electric field, tumor treatment
    Medical Specialty
    Unknown
    Advisory Committee
    Neurology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    December 3, 2012
    Date Received
    September 28, 2012
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR MODIFICATION TO THE FIELD GENERATOR COMPONENT OF THENOVOTTF-L00A SYSTEM TO REPLACE PIN: DAC7614E WITH PIN: 2IC-103572, AND CORRESPONDING CHANGES TO THE ASSOCIATED RESISTORS AND CAPACITORS TO LIMIT THE PART VOLTAGE RANGE AND ELIMINATE AN OBSERVED CURRENT SPIKE. CORRESPONDING SOFTWARE CHANGES WERE ALSO MADE TO REFLECT THESEMODIFICATIONS.

    Classifications

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

    Product Code Device Name
    NZK Stimulator, Low Electric Field, Tumor Treatment