BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ORTHOVISC

    MDR report key: 1028555 · Received April 8, 2008

    Report

    Report Number
    1223628-2008-00002
    Event Type
    Injury
    Date Received
    April 8, 2008
    Date of Event
    February 25, 2008
    Report Date
    April 8, 2008
    Manufacturer
    ANIKA THERAPEUTICS, INC.
    Product Code
    LZX
    PMA / PMN Number
    P030019
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ORTHOVISC SODIUM HYALURONATE FOR INTRA-ARTICULAR LZX ANIKA THERAPEUTICS, INC. N070058A

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Required Intervention