BEUDAMED
    FDA Adverse Event Injury Summary report: N

    10MM TI CANNULATED DISTAL FEMORAL NAIL 340MM

    MDR report key: 1081225 · Received July 15, 2008

    Report

    Report Number
    1719045-2008-00086
    Event Type
    Injury
    Date Received
    July 15, 2008
    Manufacturer
    SYNTHES MONUMENT
    Product Code
    JDS
    PMA / PMN Number
    K970733
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    NO INVESTIGATION COULD BE PERFORMED, NO CONCLUSION COULD BE DRAWN AS NO DEVICE WAS RETURNED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 10MM TI CANNULATED DISTAL FEMORAL NAIL 340MM CANNULATED NAILS JDS SYNTHES MONUMENT * 5152181

    Patients

    Seq Age Sex Outcome Treatment
    1 LOCKING BOLTS