BEUDAMED
    FDA Adverse Event Death Summary report: N

    HALL STERNUM SAW (PNEUMATIC)

    MDR report key: 223925 · Received May 12, 1999

    Report

    Report Number
    1017294-1999-00019
    Event Type
    Death
    Date Received
    May 12, 1999
    Date of Event
    December 31, 1998
    Report Date
    April 12, 1999
    Manufacturer
    LINVATEC CORP
    Product Code
    KFK
    Report Source
    Manufacturer report

    Narratives

    Description of Event or Problem · 1

    PER USER INFORMATION DURING TELEPHONE CONVERSATION--NO REPORT OF DEVICE PROBLEM DURING USE. IT WAS REPORTED THAT "THE HEART MUSCLE HAD GROWN AND ADHERED TO THE BONE".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HALL STERNUM SAW (PNEUMATIC) STERNUM SAW (PNEUMATIC) KFK LINVATEC CORP NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1