BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 77501 · Received March 18, 1997

    Report

    Report Number
    1043534-1997-00031
    Event Type
    Injury
    Date Received
    March 18, 1997
    Date of Event
    February 17, 1997
    Product Code
    HSH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION STATEMENT: THERE WAS NO DEVICE FAILURE. PRODUCT WAS MANUFACTURED AND SOLD BY DOW CORNING WRIGHT, THE ASSESTS OF WHICH WERE PURCHASED BY WRIGHT MEDICAL TECHNOLOGY, INC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * Implant HSH

    Patients

    Seq Age Sex Outcome Treatment
    1