BEUDAMED
    FDA Adverse Event Injury Summary report: N

    T2 A/R FE NAIL

    MDR report key: 534794 · Received July 15, 2004

    Report

    Report Number
    9610622-2004-00030
    Event Type
    Injury
    Date Received
    July 15, 2004
    Date of Event
    June 15, 2004
    Report Date
    June 15, 2004
    Manufacturer
    STRYKER TRAUMA KIEL/STRYKER TRAUMA GMBH KIEL OPERATIONS
    Product Code
    JDS
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE NAIL BROKE AND REQUIRED REVISION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 T2 A/R FE NAIL IMPLANT JDS STRYKER TRAUMA KIEL/STRYKER TRAUMA GMBH KIEL OPERATIONS * K781562

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Required Intervention