7 results
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16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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2520274-2013-01424
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·March 13, 2013
UNKNOWN OXFORD TIBIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·March 11, 2020
LIGHTSHEER EC
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·August 28, 2012
OXFORD UNI FEMORAL SM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·April 27, 2021
BIOMET SPINE FUSION SYSTEM
FDA Adverse Event
Injury
·BIOMET SPINE - BROOMFIELD·Product code MAX·July 1, 2016
BIOMET SPINE FUSION SYSTEM
FDA Adverse Event
Injury
·BIOMET SPINE - BROOMFIELD·Product code MAX·July 1, 2016
HANDLE CEV669B DIA 5MM ANG BIPOLAR
FDA Adverse Event
Injury
·INTEGRA MICROFRANCE S.A.S.·Product code GEI·November 12, 2019