3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TRIDENT 0 DEG CONSTRAINED INSERT 22E
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWZ·June 12, 2014
S-ROM INSRT S22, 10DEG, 22MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 12, 2010
BIPOL LEAD MODEL 300
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·December 12, 2012