BEUDAMED
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    Filters Regulation: Us FDA ×

    Ortus™ Expandable Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIALO DRAIN

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TRANS1 AXIALIF PLUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONTINUUM, TRILOGY IT, ALLOFIT IT LINER

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code KWZ·June 5, 2013

    VOYAGER? RX CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code LOX·September 19, 2008

    BONE PLATE, MP, 4 HOLE, LONG BAR

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code JEY·June 23, 2011