BEUDAMED
    FDA Adverse Event Other Summary report: N

    FOUNDATION KNEE

    MDR report key: 2214043 · Received August 2, 2011

    Report

    Report Number
    1644408-2011-00437
    Event Type
    Other
    Date Received
    August 2, 2011
    Date of Event
    July 26, 2011
    Report Date
    July 26, 2011
    Manufacturer
    ENCORE MEDICAL, L.P.
    Product Code
    JWH
    PMA / PMN Number
    K923277
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    REVISION SURGERY - THE PT FELL AND HAD A TORN MCL, PAIN IN THE KNEE AND INSTABILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FOUNDATION KNEE NON-POROUS FEMUR JWH ENCORE MEDICAL, L.P. 53897334

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Required Intervention 324-01-104, LOT 53899252| 385-09-504, LOT 53885885