6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DEFINE System (AG612444A)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Opto Wire and OptoMonitor System
FDA 510(k)
FDA Class 2
·Cardiovascular
PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
DIAMONDBACK 360 ORBITAL ATHERECTOMY SYSTEM
FDA Adverse Event
Injury
·CARDIOVASCULAR SYSTEMS, INC.·Product code MCW·November 24, 2008
FORTIFY VR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2011
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 23, 2013