BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AMC WRIST

    MDR report key: 202751 · Received December 17, 1998

    Report

    Report Number
    2219689-1998-00706
    Event Type
    Injury
    Date Received
    December 17, 1998
    Date of Event
    July 31, 1998
    Report Date
    December 16, 1998
    Manufacturer
    HOWMEDICA INC.
    Product Code
    KWN
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AMC WRIST Implant IMPLANT KWN HOWMEDICA INC. NA KGZHA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention