BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PLUS VKS

    MDR report key: 1033830 · Received April 25, 2008

    Report

    Report Number
    9612771-2008-00021
    Event Type
    Injury
    Date Received
    April 25, 2008
    Date of Event
    May 1, 2007
    Report Date
    April 24, 2008
    Manufacturer
    PLUS ORTHOPEDICS AG
    Product Code
    HSH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SZ
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO LOOSENING OF THE TIBIAL COMPONENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PLUS VKS TIBIAL COMPONENT HSH PLUS ORTHOPEDICS AG NA 054284

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Hospitalization| R