BEUDAMED
    FDA Adverse Event Other Summary report: N

    FOUNDATION KNEE SYSTEM

    MDR report key: 1061737 · Received June 16, 2008

    Report

    Report Number
    1644408-2008-00184
    Event Type
    Other
    Date Received
    June 16, 2008
    Date of Event
    May 19, 2008
    Report Date
    May 21, 2008
    Manufacturer
    ENCORE MEDICAL, L.P.
    Product Code
    HSH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    REVISION SURGERY-PATIENT HAD LIMITED RANGE OF MOTION, DOCTOR WENT TO A SMALLER INSERT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FOUNDATION KNEE SYSTEM INSERT, PRIMARY HSH ENCORE MEDICAL, L.P. 302772

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention