BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AMK TIB INS SIZE 3 10MM

    MDR report key: 1053588 · Received May 22, 2008

    Report

    Report Number
    1818910-2008-01710
    Event Type
    Injury
    Date Received
    May 22, 2008
    Date of Event
    April 25, 2008
    Report Date
    April 25, 2008
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    JWH
    PMA / PMN Number
    K864671
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    PT WAS REVISED TO ADDRESS FRACTURE OF THE TIBIAL TRAY AND POLY WEAR OF THE INSERT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AMK TIB INS SIZE 3 10MM 87JWH JWH DEPUY ORTHOPAEDICS, INC. NA 626170

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR Required Intervention