BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VITEK KENT I TOTAL JOINT

    MDR report key: 269569 · Received March 14, 2000

    Report

    Report Number
    MW1018399
    Event Type
    Injury
    Date Received
    March 14, 2000
    Date of Event
    March 7, 2000
    Report Date
    March 8, 2000
    Manufacturer
    VITEK, INC. - OOB
    Product Code
    LZD
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    REMOVAL OF IMPLANT BECAUSE OF PAIN. HAD BONE LOSS UNDER FOSSA IMPLANT AND MANDIBULAR IMPLANT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITEK KENT I TOTAL JOINT * LZD VITEK, INC. - OOB * *

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Hospitalization