BEUDAMED
    FDA Adverse Event Other Summary report: N

    2921578-2005-00002

    MDR report key: 826277 · Received July 12, 2005

    Report

    Report Number
    2921578-2005-00002
    Event Type
    Other
    Date Received
    July 12, 2005
    Date of Event
    March 1, 2005
    Report Date
    June 1, 2005
    Product Code
    FWZ
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    OFF LABEL USE BY SURGEON.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FWZ

    Patients

    Seq Age Sex Outcome Treatment
    1 WILSON FRAME.