BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CD HORIZON SPINAL SYSTEM

    MDR report key: 2768960 · Received October 2, 2012

    Report

    Report Number
    1030489-2012-01776
    Event Type
    Injury
    Date Received
    October 2, 2012
    Date of Event
    September 4, 2012
    Report Date
    September 4, 2012
    Manufacturer
    MDT SOFAMOR DANEK PUERTO RICO MFG
    Product Code
    NKB
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THIS PART IS NOT APPROVED FOR USE IN THE UNITED STATES; HOWEVER A LIKE DEVICE CATALOG # 1475005050, 510K # K102807 WAS CLEARED IN THE UNITED STATES. NEITHER THE DEVICE NOR APPLICABLE IMAGING FILMS WERE RETURNED TO THE MANUFACTURER FOR EVALUATION, THEREFORE, THE CAUSE OF THE EVENT CANNOT BE DETERMINED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT UNDERWENT A MINIMALLY INVASIVE SPINAL SURGERY AT L5-S TO TREAT STENOSIS. IT WAS REPORTED THAT THE ROD WOULD NOT PASS THROUGH BOTH SCREW HEADS ON THE LEFT SIDE. AS A RESULT, A NEW INCISION WAS ADDED TO THE PATIENT TO INSERT THE ROD, AND THE SURGEON WAS ABLE TO COMPLETE THE PROCEDURE WITHOUT ANY FURTHER INCIDENTS. PER THE REPORT, THE SURGERY TIME HAD BEEN EXTENDED ABOUT 20 MINUTES BECAUSE OF THE INCIDENT. NO ADDITIONAL PATIENT COMPLICATIONS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CD HORIZON SPINAL SYSTEM ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE NKB MDT SOFAMOR DANEK PUERTO RICO MFG NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 00068 YR Other BONE SCREWS, ROD INSERTER