10,000 results
·
53ms
·
Sources: EU EUDAMED, US FDA
LIFE SPINE
FDA Adverse Event
Injury
·LIFE SPINE·Product code MAX·October 19, 2018
LIFE SPINE INC.
FDA Adverse Event
Injury
·LIFE SPINE INC.·Product code MCV·April 18, 2008
Dyna-Link Ti
FDA UDI
Life Spine, Inc.·00190837078096·
Arx
FDA UDI
Life Spine, Inc.·00190837092757·
Hinged Laminoplasty
FDA UDI
Life Spine, Inc.·00190837103583·Neutral 10mm Parallel Plate, Hybrid Hinge
ProLift
FDA UDI
Life Spine, Inc.·00190837085964·
Gruve
FDA UDI
Life Spine, Inc.·00190837089528·Empty Gruve Sterilization Tray
Longbow Spinal System
FDA UDI
Life Spine, Inc.·00190837005795·
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837039073·3.5mm Rod Bender
Nautilus Spinal System
FDA UDI
Life Spine, Inc.·00190837053734·Nautilus Polyaxial Screw, 4.5mm x 45mm Cannulated
ARx SAI
FDA UDI
Life Spine, Inc.·00190837174019·
ARx SAI
FDA UDI
Life Spine, Inc.·00190837176112·
ProLift® Expandable Spacer System
FDA UDI
Life Spine, Inc.·00190837204488·
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837049492·Standard Plateau Tamp
Nautilus Spinal System
FDA UDI
Life Spine, Inc.·00190837057916·Non-Cannulated Screw, 4.5 x 30 Long
Arx
FDA UDI
Life Spine, Inc.·00190837074845·Polyaxial Cannulated Screw 10.5x100mm
Arx
FDA UDI
Life Spine, Inc.·00190837092665·
ProLift
FDA UDI
Life Spine, Inc.·00190837116897·
ProLift Lateral
FDA UDI
Life Spine, Inc.·00190837138592·
ARx SAI
FDA UDI
Life Spine, Inc.·00190837189204·