BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SPINAL CORD STIMULATOR (SCS)

    MDR report key: 18447183 · Received January 3, 2024

    Report

    Report Number
    MW5149797
    Event Type
    Injury
    Date Received
    January 3, 2024
    Report Date
    January 2, 2024
    Manufacturer
    NEVRO CORPORATION
    Product Code
    LGW
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT REPORTED THEY TRIED TO DO A TRIAL OF NEVRO AND ENDED UP GETTING SPINAL FLUID WHICH GAVE PATIENT A REALLY BAD HEADACHE. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    761429 SPINAL CORD STIMULATOR (SCS) STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW NEVRO CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown