BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CD HORIZON SPINAL SYSTEM

    MDR report key: 6568432 · Received May 16, 2017

    Report

    Report Number
    1030489-2017-01233
    Event Type
    Injury
    Date Received
    May 16, 2017
    Report Date
    April 20, 2017
    Manufacturer
    WARSAW ORTHOPEDICS
    Product Code
    KWP
    PMA / PMN Number
    SEE H10
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS PART IS NOT APPROVED FOR USE IN THE US, HOWEVER A LIKE DEVICE WITH PART# 869-021, 510K# K040962 AND UPN# (B)(4) IS APPROVED FOR MARKET USE. (B)(4). NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT.

    Additional Manufacturer Narrative · 1

    IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

    Description of Event or Problem · 1

    PRE-OPERATIVE DIAGNOSIS :ROD BREAKAGE IT WAS REPORTED THAT THE PATIENT UNDERWENT A POSTERIOR THORACOLUMBAR-SACRAL CORRECTION FUSION SURGERY AT T10-S2 AI USING RODS. POST-OP, THE RODS BROKE AT BOTH THE SIDES OF L3/L4. THE RODS WERE REMOVED AND REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    350056 CD HORIZON SPINAL SYSTEM APPLIANCE, FIXATION, SPINAL INTERLAMINAL KWP WARSAW ORTHOPEDICS NA 0442660W

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Required Intervention