6 results
·
23ms
·
Sources: EU EUDAMED, US FDA
BIOSPAL 2400S
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MI-750 PROCEDURAL/MINOR SURGICAL LIGHT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DETECT SURGICAL PACING AND MAPPING TOOL
FDA 510(k)
FDA Class 2
·Cardiovascular
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 30, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 20, 2012
DEPO-PROVERA¿ INJECTABLE SUSPENSION
FDA Adverse Event
Malfunction
·TEVA PHARMACEUTICAL INDUSTRIES·Product code FMF·September 3, 2010