BEUDAMED
    FDA Adverse Event Injury Summary report: N

    7.3MM CANNULATED SCREW

    MDR report key: 1032550 · Received April 11, 2008

    Report

    Report Number
    2520274-2008-00028
    Event Type
    Injury
    Date Received
    April 11, 2008
    Manufacturer
    SYNTHES
    Product Code
    HWC
    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 7.3MM CANNULATED SCREW CANNULATED SCREW HWC SYNTHES NA NI

    Patients

    Seq Age Sex Outcome Treatment
    1