3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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UNKNOWN DEPUY SROM POLY DIAL LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWY·May 15, 2014
CONSULTA CRT-P
FDA Adverse Event
Malfunction
·MEDTRONIC S.A.·Product code NVZ·October 31, 2012
SILVERBOLD SPINAL SCREW SYSTEM
FDA Adverse Event
Injury
·VERTIFLEX, INCORPORATED·Product code NQP·August 17, 2010