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

    Aortic Stent

    PMA: P240003 · Supplement: S007 · Decision Feb 11, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Aortic Stent
    Trade Name
    Minima Stent System
    PMA Number
    P240003
    Supplement Number
    S007
    Device Class
    FDA Class 3
    Product Code
    PNF
    Generic Name
    Aortic stent
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    February 11, 2026
    Date Received
    January 12, 2026
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    a change to a process inspection acceptance criterion for the balloon shaft of the Minima Stent System

    Classifications

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

    Product Code Device Name
    PNF Aortic Stent