6 results
·
26ms
·
Sources: EU EUDAMED, US FDA
THERMUFF BAG
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CONSENSUS ACETABLAR SHELL, TI COATED
FDA 510(k)
FDA Class 2
·Orthopedic
Needle Stimulator (Model: RJNS6-1)
FDA 510(k)
FDA Unclassified
·Unknown
ICHEM VELOCITY
FDA Adverse Event
Malfunction
·IRIS INTERNATIONAL·Product code KQO·July 16, 2015
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 15, 2012
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·July 8, 2014