6 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MAS PLIF Fixation system
FDA 510(k)
FDA Class 2
·Orthopedic
KENDALL SCD 700 SEQUENTIAL COMPRESSION CONTROLLER
FDA 510(k)
FDA Class 2
·Cardiovascular
TIGER HEADLESS CANNULATED SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 24, 2013
CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·August 26, 2008
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 23, 2011