8 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMITH SUBTALAR PEG
FDA 510(k)
FDA Class 1
·Orthopedic
Neodent Instrument Kit Cases
FDA 510(k)
FDA Class 2
·General Hospital
BIODRIVE MICRO SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BDRV CANN SCW SS P/T DIA4.5X60MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code HRS·January 26, 2017
BDRV CANN SCW SS P/T DIA4.5X52MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code HRS·January 26, 2017
NEUROMONITOR BASIC KIT
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC.·Product code GWM·May 6, 2014
ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·October 16, 2012
ASKU
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DTE·August 11, 2010