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

    Drug-Eluting Sinus Stent

    PMA: P100044 · Supplement: S016 · Decision May 23, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4

    Basic Information

    Device Name
    Drug-Eluting Sinus Stent
    Trade Name
    PROPEL SINUS IMPLANT AND PROPEL MINI SINUS IMPLANT
    PMA Number
    P100044
    Supplement Number
    S016
    Device Class
    FDA Class 3
    Product Code
    OWO
    Generic Name
    Drug-eluting sinus stent
    Medical Specialty
    Unknown
    Advisory Committee
    Ear, Nose, Throat
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    May 23, 2014
    Date Received
    April 23, 2014
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    ADDITION OF A NEW POUCH SEALING EQUIPMENT, SENCORP WHITE HEAT SEALER WITH VACCUUM AND GAS PURGE MODEL 12-PV/2, TO THE EXISTING MANUFACTURING LINE FOR THE PACKAGING OF THE PROPEL AND PROPEL MINI SINUS IMPLANTS.

    Classifications

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

    Product Code Device Name
    OWO Drug-Eluting Sinus Stent