9 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
ASR ACETABULAR CUPS 48
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD·Product code KWA·December 17, 2010
PS TIBIAL INSERTS SZ 4, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 14, 2023
CC FEMORAL SZ 3
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 10, 2024
CEMENTED FINNED TIB. TRA SZ 3F/3T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 19, 2024
OPTETRAK KNEE SYSTEM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 23, 2024
ROD, FIXATION, INTRAMEDULLARY
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HSB·January 22, 2017
OPTETRAK KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 29, 2024
PS TIBIAL INSERTS SZ 2, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 13, 2025
CC TIBIAL INSERT SZ 4, 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 4, 2024