BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION

    MDR report key: 1033367 · Received April 24, 2008

    Report

    Report Number
    2029203-2008-00246
    Event Type
    Injury
    Date Received
    April 24, 2008
    Date of Event
    March 26, 2008
    Report Date
    March 25, 2008
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION CORP
    Product Code
    LGW
    PMA / PMN Number
    P030017
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE IPG AND LEAD EXTENSIONS WERE DISCARDED BY THE MEDICAL FACILITY AND WILL NOT BE RETURNED FOR EVAL.

    Description of Event or Problem · 1

    THE PT'S IMPLANT AND LEAD EXTENSIONS WERE EXPLANTED DUE TO SKIN EROSION. THE PT IS REPORTEDLY DOING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION SPINAL CORD STIMULATOR LGW BOSTON SCIENTIFIC NEUROMODULATION CORP SC-1110 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention SC-3108-25 EXPLANTED| SC-3138-25 EXPLANTED