BEUDAMED
    FDA Adverse Event Other Summary report: N

    MENISCUS ARROW

    MDR report key: 380963 · Received January 16, 2002

    Report

    Report Number
    9613278-2002-00004
    Event Type
    Other
    Date Received
    January 16, 2002
    Date of Event
    March 10, 2000
    Report Date
    August 24, 2001
    Manufacturer
    BIONX IMPLANTS, LTD.
    Product Code
    MAI
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    PART OF MENISCUS ARROW REMOVED 14 MONTHS POSTOPERATIVELY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MENISCUS ARROW BIOABSORBABLE SOFT TISSUE FIXATION DEVICE MAI BIONX IMPLANTS, LTD. 521113 978

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention