7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
M. KUROSAKA INTERFERENCE FIXATION SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
Ventura NanoMetalene System
FDA UDI
Seaspine Orthopedics Corporation·10889981151935·Ventura NM Trial, 11mm x 24mm x 10mm, Lordotic
NOVOFINE PLUS 32G 4 MM
FDA 510(k)
FDA Class 2
·General Hospital
MONITORING SYSTEM, MODEL ARGUS PB-2200
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 29, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 16, 2010
ENDEAVOR SPRINT RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·July 15, 2014