11 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TOTAL FEMUR
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE·Product code KRO·June 7, 2018
CUSTOM TOTAL FEMUR REPLACEMENT IMPLANT
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014
ARTICULEZE M HEAD 36MM +8.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 26, 2013
CAPSUREFIX
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code DTB·March 16, 2011
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWP·March 28, 2008
CUSTOM TOTAL FEMUR REPLACEMENT
FDA Adverse Event
Malfunction
·STANMORE IMPLANTS WORLDWIDE LTD·Product code JDI·July 24, 2015
CUSTOM TOTAL FEMORAL REPLACEMENT IMPLANT
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE LTD·Product code JDI·December 23, 2014
CUSTOM TOTAL FEMUR REPLACEMENT IMPLANT
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·December 1, 2014
PROXIMAL FEMUR
FDA Adverse Event
Malfunction
·STANMORE IMPLANTS WORLDWIDE LTD·Product code JDI·December 23, 2014
PATIENT SPECIFIC TOTAL FEMUR
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE·Product code KRO·August 15, 2018
FEM KNEE W/EPI R SM
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE·Product code KRO·January 16, 2020