BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Catheter, Coronary, Atherectomy

    PMA: P900056 · Supplement: S009 · Decision Aug 14, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22

    Basic Information

    Device Name
    Catheter, Coronary, Atherectomy
    Trade Name
    ROTABLATOR(R)
    PMA Number
    P900056
    Supplement Number
    S009
    Device Class
    FDA Class 3
    Product Code
    MCX
    Generic Name
    CATHETER, CORONARY, ATHERECTOMY
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    August 14, 1995
    Date Received
    December 8, 1994
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Location Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    CHANGE IN LOCATION FOR SEAMED CORPORATION, THE MANUFACTURER OF THE CONSOLE USED WITH THE ROTABLATOR SYSTE, FROM 11810 NORTH CREEK PARKWAY NORTH, BOTHELL, WASHINGTON, TO WEST WILLOWS TECHNOLOGY CENTER, N.E. 87TH STREET, REDMOND, WASHINGTON

    Classifications

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

    Product Code Device Name
    MCX Catheter, Coronary, Atherectomy