10,000 results
·
38ms
·
Sources: EU EUDAMED, US FDA
LIFE SPINE
FDA Adverse Event
Malfunction
·LIFE SPINE·Product code MAX·February 1, 2018
LIFE SPINE
FDA Adverse Event
Malfunction
·LIFE SPINE·Product code OVD·April 27, 2018
LIFE SPINE
FDA Adverse Event
Malfunction
·LIFE SPINE·Product code KWQ·April 27, 2018
LIFE SPINE
FDA Adverse Event
Malfunction
·LIFE SPINE, INC.·Product code MAX·October 21, 2019
LIFE SPINE INC.
FDA Adverse Event
Injury
·LIFE SPINE INC.·Product code MCV·April 18, 2008
Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System
FDA 510(k)
FDA Class 2
·Orthopedic
LIFE SPINE MODIFICATION TO LIFE SPINE NEO ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·LIFE SPINE·Product code KWQ·January 4, 2013
PROLIFT MICRO
FDA Adverse Event
Injury
·LIFE SPINE·Product code MAX·October 16, 2023
LIFESPINE
FDA Adverse Event
Injury
·LIFE SPINE, INC.·Product code MAX·August 20, 2020
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·