7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
CEEGRAPH, MODIFICATION
FDA 510(k)
FDA Class 2
·Neurology
SeaSpine Spacer System - Pacifica™
FDA UDI
Seaspine Orthopedics Corporation·10889981032340·Pacifica Trial 11mm x 20mm x 10mm
LACTOSORB TIBIAL L-15 SCREW AND WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
PJUR ORIGINAL, PJUR WOMAN, PJUR MAN EXTREME GLIDE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ABSOLUTE .035 SELF EXPANDING STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code FGE·January 29, 2013
PROGENIX PLUS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MBP·December 20, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 14, 2014