BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MATRIX DETACHABLE COILS

    MDR report key: 1694193 · Received May 19, 2010

    Report

    Report Number
    2939204-2010-00511
    Event Type
    Injury
    Date Received
    May 19, 2010
    Date of Event
    April 26, 2006
    Report Date
    April 26, 2006
    Manufacturer
    BOSTON SCIENTIFIC - CORK
    Product Code
    HCG
    PMA / PMN Number
    UNKNOWN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ES
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    PMA# OR 510K#: K012985; K031168 AND K050700. FOR ANTICIPATED PROCEDURAL COMPLICATION.. THE DEVICE REMAINS IMPLANTED AND WAS NOT AVAILABLE FOR ANALYSIS. FROM THE INFORMATION PROVIDED THERE WAS NO INDICATION THAT THE DEVICE WAS NOT USED AS IN ACCORDANCE WITH THE LABELING OR THAT THIS CAUSED OR CONTRIBUTED TO THE REPORTED EVENT. REVASCULARIZATION AND INADEQUATE OCCLUSION ARE KNOWN AND ANTICIPATED COMPLICATIONS TO THESE TYPES OF PROCEDURES AND ARE NOTED IN THE LABELING. MULTIPLE EMBOLIZATION PROCEDURES MAY BE REQUIRED TO ACHIEVE THE DESIRED OCCLUSION OF SOME ANEURYSMS OR VESSELS. THEREFORE, IT WAS DETERMINED THAT THE REPORTED EVENT WAS AN ANTICIPATED PROCEDURAL COMPLICATION.

    Description of Event or Problem · 1

    THE PATIENT UNDERWENT THE SUCCESSFUL COIL EMBOLIZATION OF THE LEFT OPHTHALMIC ARTERY ANEURYSM. THE NUMBER AND MODEL OF THE COILS IMPLANTED WAS NOT DISCLOSED. APPROXIMATELY ELEVEN MONTHS POST PROCEDURE; THE PATIENT UNDERWENT A SECOND PROCEDURE TO TREAT THE REOCCURRENCE OF THE ANEURYSM. NO OTHER INFORMATION WAS PROVIDED

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MATRIX DETACHABLE COILS DEVICE, NEUROVASCULAR EMBOLIZATION HCG BOSTON SCIENTIFIC - CORK UNK536

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Required Intervention