BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INTERNAL MIDFACE DISTRACTOR, 20MM

    MDR report key: 2971637 · Received February 21, 2013

    Report

    Report Number
    0008010177-2013-00004
    Event Type
    Injury
    Date Received
    February 21, 2013
    Date of Event
    January 2, 2013
    Report Date
    January 2, 2013
    Manufacturer
    STRYKER OSTEOSYNTHESIS-FREIBURG
    Product Code
    JEY
    PMA / PMN Number
    K092743
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    OTHER
    Health Professional
    *

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    77490 INTERNAL MIDFACE DISTRACTOR, 20MM INSTRUMENT JEY STRYKER OSTEOSYNTHESIS-FREIBURG

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown