BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STEFFEE VSP SPINAL IMPLANT

    MDR report key: 18228 · Received December 5, 1994

    Report

    Report Number
    MW1004326
    Event Type
    Injury
    Date Received
    December 5, 1994
    Date of Event
    August 24, 1989
    Report Date
    November 15, 1994
    Manufacturer
    AOMED CORP.
    Product Code
    MCV
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    LOWER BACK PAIN, UPPER BACK PAIN, HEADACHES (LEFT SIDE, DURATION: 2 HRS TO ALL NIGHT), WALKING AND SPINAL CORD PAIN, LEFT LEG PAIN AND LEFT ARM PAIN, KIDNEY PAIN AND LEFT FOOT PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STEFFEE VSP SPINAL IMPLANT Implant SPINAL IMPLANT MCV AOMED CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR Disability