BEUDAMED
    FDA Adverse Event Other Summary report: N

    MENISCUS ARROW

    MDR report key: 371366 · Received January 7, 2002

    Report

    Report Number
    9613278-2001-00022
    Event Type
    Other
    Date Received
    January 7, 2002
    Date of Event
    December 27, 2000
    Report Date
    March 26, 2001
    Manufacturer
    BIONX IMPLANTS, LTD.
    Product Code
    MAI
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PART OF MENISCUS ARROW WAS REMOVED 7 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 1869

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention