BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2182207-2009-07584

    MDR report key: 23776583 · Received March 11, 2009

    Report

    Report Number
    2182207-2009-07584
    Event Type
    Injury
    Date Received
    March 11, 2009
    Date of Event
    February 16, 2009
    Report Date
    March 11, 2009
    Manufacturer
    MEDTRONIC NEUROMODULATION
    PMA / PMN Number
    P960009
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention