BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CORMET RESURFACING

    MDR report key: 4543396 · Received May 6, 2014

    Report

    Report Number
    9614209-2014-00039
    Event Type
    Injury
    Date Received
    May 6, 2014
    Date of Event
    January 19, 2012
    Report Date
    May 6, 2014
    Manufacturer
    CORIN LTD.
    Product Code
    NXT
    PMA / PMN Number
    P050016
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4) INITIAL REPORT. DEVICE DETAILS, PT MED HISTORY, POST PRIMARY AND PRE REVISION X RAYS, EXPLANT AND REASON FOR REVISION HAVE BEEN REQUESTED IN ORDER TO PROGRESS WITH THE INVESTIGATION. DEVICE MFG RECORDS TO BE REVIEWED. PLEASE NOTE: THIS REPORT IS FILED WITH THE FDA DUE TO AN EVENT EXPERIENCED WITH A DEVICE THAT IS SIMILAR TO THOSE PLACED ON THE MARKET IN THE USA; HOWEVER, THIS EVENT OCCURRED OUTSIDE OF THE USA.

    Description of Event or Problem · 1

    CORMET REVISION AFTER 5 YEARS 7 MONTHS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    273193 CORMET RESURFACING NXT CORIN LTD. 179.2508 JWGR

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention ASSOCIATED CORMET HEAD 179.044B LOT JUVZ