BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRINITY ACETABULAR SYSTEM

    MDR report key: 2492532 · Received March 14, 2012

    Report

    Report Number
    9614209-2012-00001
    Event Type
    Injury
    Date Received
    March 14, 2012
    Report Date
    December 14, 2011
    Manufacturer
    CORIN LTD.
    Product Code
    MEH
    PMA / PMN Number
    K0093472
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    PT WAS REVISED AFTER 4 WEEK DUE TO LINER FRACTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRINITY ACETABULAR SYSTEM MEH PROST HIP SEMI-CONST MEH CORIN LTD. UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R