BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    IMPACT MODEL 316

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690121909·Femoral Posterior Augment Trial, Sz 2+, 5mm

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690121312·Femoral Augment Posterior, Size 2+, 5mm

    Montage Settable Bone Putty

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NUVASIVE COROENT SMALL CONTOURED INTERBODY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRESIDIO 18 - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·May 31, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 21, 2012

    NEUROMONITOR BASIC KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC., MEDOS S.A.·Product code GWM·September 21, 2010