BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INFUSE BONE GRAFT

    MDR report key: 3180535 · Received June 20, 2013

    Report

    Report Number
    1030489-2013-02438
    Event Type
    Injury
    Date Received
    June 20, 2013
    Report Date
    September 26, 2016
    Manufacturer
    MEDTRONIC SOFAMOR DANEK USA, INC
    Product Code
    NEK
    PMA / PMN Number
    P000058
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). (B)(6). NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT.

    Additional Manufacturer Narrative · 1

    A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY A NON-MEDICAL PROFESSIONAL THAT THE PATIENT UNDERWENT A PROCEDURE FOR BILATERAL REVISION LAMINECTOMY, FORAMINOTOMY, AND FACETECTOMY, AS WELL AS A L3-4, L4-5 POSTERIOR LUMBAR FUSION AND INSTRUMENTATION REMOVAL AT L4-5. RHBMP WAS IMPLANTED WITH A PEEK CAGE VIA A POSTERIOR APPROACH. ALLEGEDLY, THE PATIENT HAS REQUIRED EXTENSIVE MEDICAL TREATMENT AND CONTINUES TO SUFFER FROM CHRONIC PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    281154 INFUSE BONE GRAFT FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET NEK MEDTRONIC SOFAMOR DANEK USA, INC NA M110809AAA

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Required Intervention