BEUDAMED
    FDA Adverse Event Other Summary report: N

    SILHOUETTE SPINAL FIXATION SYSTEM

    MDR report key: 889554 · Received August 19, 2004

    Report

    Report Number
    2184052-2004-00012
    Event Type
    Other
    Date Received
    August 19, 2004
    Date of Event
    July 16, 2004
    Report Date
    August 19, 2004
    Manufacturer
    ZIMMER SPINE, INC.
    Product Code
    MCV
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SILHOUETTE SPINAL FIXATION SYSTEM SILHOUETTE POLYAXIAL PEDICLE SCREW MCV ZIMMER SPINE, INC. 7220-6555-00 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Other