BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PFC SIGMARP STB IN 3 10.0

    MDR report key: 1885144 · Received October 22, 2010

    Report

    Report Number
    1818910-2010-07446
    Event Type
    Injury
    Date Received
    October 22, 2010
    Date of Event
    September 30, 2010
    Report Date
    September 30, 2010
    Manufacturer
    DEPUY INTL., LTD.
    Product Code
    NJL
    PMA / PMN Number
    P830055/S074
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    PT REVISED FOR PAIN AND STIFFNESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PFC SIGMARP STB IN 3 10.0 87 NJL NJL DEPUY INTL., LTD. NA 225252

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Required Intervention