BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FLANGE FIXTURE AND ABUTMENT

    MDR report key: 3110139 · Received May 13, 2013

    Report

    Report Number
    6000034-2013-00853
    Event Type
    Injury
    Date Received
    May 13, 2013
    Date of Event
    March 27, 2013
    Report Date
    May 3, 2013
    Manufacturer
    COCHLEAR BONE ANCHORED SOLUTIONS AB
    Product Code
    LXB
    PMA / PMN Number
    K955713
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    AUDIOLOGIST

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). IMPLANTED DEVICE REMAINS.

    Description of Event or Problem · 1

    PER THE CLINIC, THE PATIENT RECEIVED AN INJECTION AT THE IMPLANT SITE (KENALOG) TO TREAT KELOID GROWTH. THE IMPLANTED DEVICE REMAINS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    210238 FLANGE FIXTURE AND ABUTMENT LXB LXB COCHLEAR BONE ANCHORED SOLUTIONS AB 93331

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention