BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN

    MDR report key: 1516478 · Received October 21, 2009

    Report

    Report Number
    2182207-2009-07635
    Event Type
    Injury
    Date Received
    October 21, 2009
    Date of Event
    February 14, 2009
    Report Date
    March 11, 2009
    Manufacturer
    MEDTRONIC NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    UNK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    EZ
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT IS BEING SUBMITTED FOLLOWING AN INTERNAL ASSESSMENT.

    Description of Event or Problem · 1

    LITERATURE: VRBA I, KOZAK J, KORAN M, KNOTEK P, STETKAROVA I. [BIO-PSYCHO-SOCIAL ASSESSMENT OF NEUROMODULATION ANALGESIC TREATMENT OF PTS WITH FAILED BACK SURGERY SYNDROME (FIRST PART)]. BOLEST. IN 2008; 11(4):207-214. SUMMARY: THIS ARTICLE PRESENTS THE USE OF NEUROMODULATION ANALGESIC METHODS (BOTH STIMULATION AND DRUG DELIVERY) FOR THE TREATMENT OF FAILED BACK SURGERY SYNDROME (FBSS) IN 36 PTS, WHO FAILED CONVENTIONAL MEDICATION MANAGEMENT AND SUCCESSFULLY FULFILLED THE TRIAL PERIOD. TWENTY-FOUR PTS WERE IMPLANTED WITH NEUROSTIMULATION SYSTEMS WITH ONE ELECTRODE, 2 PTS WERE IMPLANTED WITH NEUROSTIMULATION SYSTEMS WITH TWO ELECTRODES, AND 12 PTS WERE IMPLANTED WITH A PUMP SYSTEM. REPORTABLE EVENT: TWO PTS EXPERIENCED SERIOUS INFECTIONS REQUIRING REMOVAL OF THE SYSTEM. NO PT OUTCOME WAS REPORTED. SEE LITERATURE ARTICLE WITH MFR REPORT # 2182207200907575.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNKNOWN UNKNOWN LGW MEDTRONIC NEUROMODULATION UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention