BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2021898-2007-00048

    MDR report key: 831023 · Received March 13, 2007

    Report

    Report Number
    2021898-2007-00048
    Event Type
    Malfunction
    Date Received
    March 13, 2007
    Product Code
    JXG
    PMA / PMN Number
    K902783
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT YET BEEN RETURNED TO THE MFR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JXG

    Patients

    Seq Age Sex Outcome Treatment
    1