BEUDAMED
    FDA Adverse Event Other Summary report: N

    NATURAL KNEE II TIBIAL INSERT IMPACTOR HEAD

    MDR report key: 36145 · Received August 27, 1996

    Report

    Report Number
    2935620-1996-00001
    Event Type
    Other
    Date Received
    August 27, 1996
    Date of Event
    August 5, 1996
    Report Date
    August 8, 1996
    Manufacturer
    INTERMEDICS ORTHOPEDICS, INC.
    Product Code
    HSH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INSTRUMENT BROKE WHILE IMPACTING INSERT CAUSING A SURGICAL DELAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NATURAL KNEE II TIBIAL INSERT IMPACTOR HEAD KNEE PROSTHESIS INSTRUMENTATION HSH INTERMEDICS ORTHOPEDICS, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Other