BEUDAMED
    FDA Adverse Event Other Summary report: N

    NATURAL KNEE II NON-POROUS FEMORAL RT S25

    MDR report key: 47488 · Received November 7, 1996

    Report

    Report Number
    2935620-1996-00008
    Event Type
    Other
    Date Received
    November 7, 1996
    Date of Event
    October 8, 1996
    Report Date
    November 6, 1996
    Manufacturer
    INTERMEDICS ORTHOPEDICS, INC.
    Product Code
    HSA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NOTICE TO MFR OF SURGICAL DELAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NATURAL KNEE II NON-POROUS FEMORAL RT S25 Implant KNEE IMPLANT PROSTHESIS HSA INTERMEDICS ORTHOPEDICS, INC. NA 1253813-A

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Other