59 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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NEXGEN FEMORAL COMPONENT OPTION FOR CEMENTED USE ONLY SIZE E LEFT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021
PERSONA ARTICULAR SURFACE WITH HINGE POST EXTENSION SIZE E 20 MM HEIGHT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021
PERSONA ARTICULAR SURFACE WITH SEGMENTAL HINGE POST SIZE E 20 MM HEIGHT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2021
RIGHT SIZE E CEMENTED OPTION FEMORAL COMPONENT FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2023
NEXGEN FEMORAL AUGMENTS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018
NEXGEN FEMORAL AUGMENTS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 4, 2018
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 9, 2016
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
ADAPTA D
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·November 10, 2014
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 5, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·February 6, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015