BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AEQUALIS

    MDR report key: 3133801 · Received May 23, 2013

    Report

    Report Number
    9610667-2013-00110
    Event Type
    Injury
    Date Received
    May 23, 2013
    Date of Event
    October 11, 2007
    Report Date
    March 26, 2013
    Manufacturer
    TORNIER SAS
    Product Code
    KWS
    PMA / PMN Number
    K060209
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IS THE INITIAL REPORT SUBMITTED REGARDING THIS SURGICAL EVENT AND MEDICAL DEVICE.

    Description of Event or Problem · 1

    INTRA OP, GLENOID FRACTURE, SYNTHESE SCREWS WITH HUMERAL HAD BONE GRAFT, SURGICAL FRACTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    229037 AEQUALIS NONE KWS TORNIER SAS DWB216

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Required Intervention