BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LCP 4.5/5 BROAD 18HO L332 TI

    MDR report key: 2870797 · Received December 12, 2012

    Report

    Report Number
    2520274-2012-03756
    Event Type
    Injury
    Date Received
    December 12, 2012
    Date of Event
    November 15, 2008
    Report Date
    February 15, 2010
    Manufacturer
    SYNTHES
    Product Code
    KTT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE WAS USED FOR TREATMENT. THE PMA/501K NUMBER FOR THIS DEVICE IS K000682. THIS INDIVIDUAL ADVERSE EVENT REPORT IS BEING MADE IN ACCORDANCE WITH THE SYNTHES MDR EXEMPTION REQUEST DATED OCTOBER 2011. A REVIEW OF THE EVENTS ASSOCIATED WITH THE REQUEST WAS PERFORMED AND IT WAS DETERMINED THAT NONE OF THE EVENTS CONSTITUTES SYSTEMIC ISSUES RELATED TO PRODUCT QUALITY, CHANGES IN PRODUCT DESIGN, METHOD OF USE, OR CHANGES IN EXPECTED RISK THRESHOLDS. REVIEW OF THE DATA ALSO INDICATED NO SIGNIFICANT CHANGE IN RISK/BENEFIT OF EACH PRODUCT CATEGORY, NO EVIDENCE OF DEFICIENCIES IN THE DESIGN, LABELING, OR MANUFACTURE OF THE DEVICE. AS NO LOT NUMBER WAS PROVIDED, NO DEVICE HISTORY RECORD REVIEW CAN BE PERFORMED. THE DEVICE IS NOT BEING RETURNED FOR EVALUATION, NO FURTHER INFORMATION IS AVAILABLE ON THIS EVENT. NO FURTHER INVESTIGATION CAN BE PERFORMED.

    Description of Event or Problem · 1

    THE EU COMPLAINT HANDLING UNIT REPORTED THAT A PLATE BROKE THREE WEEKS POST-OPERATIVELY. THE PATIENT HAD A FEMUR FRACTURE AND WAS TREATED WITH LOCKING COMPRESSION PLATE ON (B)(6) 2008. THE PATIENT WAS SUBSEQUENTLY REVISED. THE PATIENT'S LAWYER CLAIMS FOR COMPENSATION AND NO PRODUCT WAS RECEIVED FOR INVESTIGATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LCP 4.5/5 BROAD 18HO L332 TI LOCKING COMPRESSION PLATE KTT SYNTHES

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention