277 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·June 14, 2013
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·July 26, 2012
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·July 26, 2012
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 24, 2012
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·June 14, 2013
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·February 5, 2014
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 5, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 21, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 5, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·April 16, 2019
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 6, 2011