BEUDAMED
    FDA Adverse Event Other Summary report: N

    MICRO-LOK IMPLANT

    MDR report key: 183578 · Received August 20, 1998

    Report

    Report Number
    1045056-1997-04706
    Event Type
    Other
    Date Received
    August 20, 1998
    Date of Event
    November 24, 1997
    Report Date
    December 15, 1997
    Manufacturer
    BIO-LOK INTL.
    Product Code
    DZE
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IMPLANT FAILED TO OSSEOINTEGRATE DUE TO STEROID THERAPY AND OTHER MEDICAL PROBLEMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICRO-LOK IMPLANT Implant CYLINDER IMPLANT DZE BIO-LOK INTL. IHCSTP313 9603140786

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other