BEUDAMED
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    MEDTRONIC MODEL 3550 ACCESSORY KIT (CONTENTS) 3550-OX

    FDA 510(k)
    FDA Class 2 ·Neurology

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233459·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY CURVED 2...

    Keos Lumbar IBFD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOGRAPH 64 AND BIOGRAPH 40

    FDA 510(k)
    FDA Class 2 ·Radiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 25, 2013

    UV-FLASH SOLUTION TRANSFER SET(SHORT) - JAPAN

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·January 13, 2011

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 21, 2014

    Depuy P.F.C. E Knee System, all polyethylene curved tibial component, Sz 2.5, 10 mm; Ref 96-0631.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005