BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ADVANCER II MEDIAL-PIVOT TIBIAL INSERT

    MDR report key: 1012640 · Received March 13, 2008

    Report

    Report Number
    1043534-2008-00026
    Event Type
    Injury
    Date Received
    March 13, 2008
    Report Date
    February 28, 2008
    Manufacturer
    *
    Product Code
    JWH
    PMA / PMN Number
    K972770
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION IS NOT COMPLETE. PRODUCT NOT RETURNED FOR EVALUATION. TRENDS WILL BE EVALUATED. THIS REPORT WILL BE AMENDED WHEN THE INVESTIGATION IS COMPLETED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANCER II MEDIAL-PIVOT TIBIAL INSERT JWH JWH * * 026319288

    Patients

    Seq Age Sex Outcome Treatment
    1 *