BEUDAMED
    FDA Adverse Event Death Summary report: N

    BAK INSTRUMENTATION

    MDR report key: 232869 · Received July 22, 1999

    Report

    Report Number
    2184052-1999-00005
    Event Type
    Death
    Date Received
    July 22, 1999
    Date of Event
    June 3, 1999
    Report Date
    July 22, 1999
    Manufacturer
    SULZER SPINE-TECH
    Product Code
    LXH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    SURGICAL COMPLICATIONS RESULTED IN DEATH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BAK INSTRUMENTATION DRILL TUBE LXH SULZER SPINE-TECH NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Death| L| R