BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Intracranial Aneurysm Flow Diverter

    PMA: P100018 · Supplement: S052 · Decision Feb 20, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Intracranial Aneurysm Flow Diverter
    Trade Name
    PIPELINE EMBOLIZATION DEVICE
    PMA Number
    P100018
    Supplement Number
    S052
    Device Class
    FDA Class 3
    Product Code
    OUT
    Generic Name
    Intracranial aneurysm flow diverter
    Medical Specialty
    Unknown
    Advisory Committee
    Neurology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    February 20, 2026
    Date Received
    November 20, 2025
    Supplement Type
    Real-Time Process
    Supplement Reason
    Labeling Change - Indications/instructions/shelf life/tradename
    Expedited Review
    N

    Advisory Committee Statement

    Approval of claims regarding reduced material thrombogenicity of a proprietary surface modification for the Pipeline™ Flex Embolization Device with Shield Technology™ and Pipeline™ Vantage Embolization Device with Shield Technology™ supported by acute benchtop in-vitro testing.

    Classifications

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

    Product Code Device Name
    OUT Intracranial Aneurysm Flow Diverter