BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6.2MM TI CLICK'X PEDICLE SCREW DUAL CORE 40MM THREAD LENGTH

    MDR report key: 2061271 · Received April 11, 2011

    Report

    Report Number
    1719045-2011-00163
    Event Type
    Injury
    Date Received
    April 11, 2011
    Report Date
    March 30, 2011
    Manufacturer
    SYNTHES MONUMENT
    Product Code
    NKB
    PMA / PMN Number
    K082572
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL INFORMATION HAS BEEN REQUESTED. INVESTIGATION IS ONGOING; NO CONCLUSION COULD BE DRAWN AS NO DEVICE WAS RETURNED OR LOT NUMBER PROVIDED. SYNTHES IS UNABLE TO DETERMINE MANUFACTURING DATE. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

    Description of Event or Problem · 1

    PATIENT IMPLANTED WITH CLICK'X HARDWARE AT L4-L5 (B)(6) 2005. HARDWARE WAS REMOVED ON (B)(6) 2011 TO REPAIR AN ADJACENT LEVEL ISSUE WITH DISC DEGENERATION. PATIENT REVISED TO HARDWARE AT L3-L4. THERE WAS NO ISSUE WITH THE CLICK'X HARDWARE. HARDWARE WAS ONLY REMOVED TO REPAIR ADJACENT LEVEL. THIS IS THE 3RD OF 14 REPORTS SUBMITTED ON THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 6.2MM TI CLICK'X PEDICLE SCREW DUAL CORE 40MM THREAD LENGTH CLICK'X PEDICLE SCREW NKB SYNTHES MONUMENT NA NI

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention LOCKING CAPS| RODS| SCREWS| 3D HEADS