BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OSTEOMED

    MDR report key: 93544 · Received May 27, 1997

    Report

    Report Number
    2027754-1997-00024
    Event Type
    Malfunction
    Date Received
    May 27, 1997
    Report Date
    May 22, 1997
    Manufacturer
    OSTEOMED CORP.
    Product Code
    HWC
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OSTEOMED Implant 1.2 X 6MM SCREW HWC OSTEOMED CORP. NA NI

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO