6 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
K012364
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 3, 2015
DELTA CER HEAD 11/13 32MM +6
FDA Adverse Event
Injury
·DEPUY IRELAND 9616671·Product code LZO·August 5, 2014
DELTA CER INSERT 36ID X 62OD
FDA Adverse Event
Injury
·DEPUY IRELAND 9616671·Product code MRA·August 5, 2014
DELTA CER HEAD 11/13 36MM +9
FDA Adverse Event
Injury
·DEPUY IRELAND 9616671·Product code LZO·August 5, 2014
IMPLANTABLE PACING LEAD
FDA Adverse Event
Injury
·MEDTRONIC, B.V.·Product code DTB·October 31, 2012
SUPER POLI-GRIP
FDA Adverse Event
Injury
·Product code KOL·August 18, 2010