7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MEDTRONIC 3465 SE-4F RECEIVER/EXTENSION FOR SPINAL
FDA 510(k)
FDA Class 2
·Neurology
CULTROL-ANTIBIOTIC/ANTIMYCOTIC SOLUT
FDA 510(k)
FDA Class 1
·Microbiology
PFC MODULAR KNEE SYSTEM CRUCIATE RETAINING TIBIAL TRAY
FDA Adverse Event
Injury
·JOHNSON & JOHNSON PROFESSIONALS, INC.·Product code HSH·May 15, 1997
PROMUS ELEMENT? PLUS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 10, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·October 11, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012