9 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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UNIV 2-HOLE SHL 56MM LNR SZ 24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·March 12, 2013
PAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code GZB·February 15, 2008
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 25, 2012
REVISION
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·September 14, 2020
AXLE LARGE
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code JDB·September 29, 2023
FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020
INDUCTOS
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·November 16, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 22, 2021
PROCLEIX ULTRIO ELITE ASSAY
FDA Adverse Event
Injury
·GRIFOLS DIAGNOSTIC SOLUTIONS INC.·Product code QHO·March 1, 2024