BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROSTHESIS, HIP COMPONENT

    MDR report key: 1060564 · Received June 6, 2008

    Report

    Report Number
    1825034-2008-00169
    Event Type
    Injury
    Date Received
    June 6, 2008
    Date of Event
    April 8, 2008
    Report Date
    May 12, 2008
    Product Code
    KWY
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CO, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PROSTHESIS, HIP COMPONENT KWY

    Patients

    Seq Age Sex Outcome Treatment
    1