BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASCEND

    MDR report key: 3133730 · Received May 23, 2013

    Report

    Report Number
    3004983210-2013-00011
    Event Type
    Injury
    Date Received
    May 23, 2013
    Date of Event
    May 16, 2012
    Report Date
    March 26, 2013
    Manufacturer
    TORNIER INC
    Product Code
    HSD
    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, NONE (POSTERIOR), SURGICAL FRACTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    229717 ASCEND NONE HSD TORNIER INC

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Required Intervention