3 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
S-ROM M HEAD 36MM -3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 27, 2014
UNKNOWN M2A CUP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·November 15, 2012
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·September 9, 2010