BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ORTHOLOC ADVANTIM TIBIAL BASE

    MDR report key: 77626 · Received March 18, 1997

    Report

    Report Number
    1043534-1997-00029
    Event Type
    Injury
    Date Received
    March 18, 1997
    Date of Event
    February 17, 1997
    Product Code
    JWH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION STATEMENT: NO CONCLUSION CAN BE DRAWN. PRODUCT WAS MANUFACTURED AND SOLD BY DOW CORNING WRIGHT, THE ASSETS OF WHICH WERE PURCHASED BY WRIGHT MEDICAL TECHNOLOGY, INC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ORTHOLOC ADVANTIM TIBIAL BASE Implant KNEE COMPONENT-DEVICE 1 JWH NA 072M735870

    Patients

    Seq Age Sex Outcome Treatment
    1