BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEXUS SPINE

    MDR report key: 24760871 · Received April 1, 2026

    Report

    Report Number
    3011390763-2026-00002
    Event Type
    Injury
    Date Received
    April 1, 2026
    Date of Event
    February 25, 2026
    Report Date
    April 28, 2026
    Manufacturer
    NEXUS SPINE, LLC
    Product Code
    NKB
    PMA / PMN Number
    K223529
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT UNDERWENT REVISION SURGERY FOR THE REMOVAL AND REPLACEMENT OF FIXED LENGTH COUPLER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    599112 NEXUS SPINE INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION NKB NEXUS SPINE, LLC 520284 115702

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Female Other