BEUDAMED
    FDA Adverse Event Death Summary report: N

    VLIFT CAGE DIAM 22 X 37 MM

    MDR report key: 1103043 · Received August 8, 2008

    Report

    Report Number
    9617544-2008-00721
    Event Type
    Death
    Date Received
    August 8, 2008
    Date of Event
    June 6, 2008
    Report Date
    July 15, 2008
    Manufacturer
    STRYKER SPINE
    Product Code
    MQP
    PMA / PMN Number
    k060506
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VLIFT CAGE DIAM 22 X 37 MM IMPLANT MQP STRYKER SPINE NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Death