BEUDAMED
    FDA Adverse Event Summary report: N

    SPINAL FIXATION DEVICE

    MDR report key: 1873768 · Received September 23, 2010

    Report

    Report Number
    1526439-2010-00135
    Date Received
    September 23, 2010
    Manufacturer
    DEPUY SPINE, INC.
    Product Code
    MNH
    PMA / PMN Number
    K062174
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE 2: SEE 1526439-2010-00134.

    Description of Event or Problem · 1

    DEVICE 2 - SEE 1526439-2010-00134.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SPINAL FIXATION DEVICE MNH DEPUY SPINE, INC. NA

    Patients

    Seq Age Sex Outcome Treatment
    1