BEUDAMED
    FDA Adverse Event Other Summary report: N

    MENISCUS ARROW

    MDR report key: 371381 · Received January 7, 2002

    Report

    Report Number
    9613278-2001-00016
    Event Type
    Other
    Date Received
    January 7, 2002
    Date of Event
    May 17, 1999
    Report Date
    August 24, 2001
    Manufacturer
    BIONX IMPLANTS LTD.
    Product Code
    MAI
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    TWO MONTHS POSTOPERATIVELY INTRA-ARTICULAR LOOSE BODY (DISLODGED MENISCAL ARROW) WAS REMOVED. INITIALLY POSTERIOR HORN OF THE LATERAL MENISCUS WAS FIXED WITH THIS DEVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MENISCUS ARROW BIOABSORBABLE SOFT TISSUE FIXATION DEVICE MAI BIONX IMPLANTS LTD. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention