BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2182596-1997-00453

    MDR report key: 116102 · Received August 28, 1997

    Report

    Report Number
    2182596-1997-00453
    Event Type
    Injury
    Date Received
    August 28, 1997
    Date of Event
    June 16, 1997
    Product Code
    FTR
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1