7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIORCI SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
SPECTRANETICS QUICK CROSS EXTREME SUPPORT CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
Streamline MIS Spinal Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
LAP-BAND ADJUSTABEL GASTRIC BANDING SYSTEM (UNK SIZE)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·March 1, 2013
MEDTRONIC LEAD
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code DXY·August 8, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
UNKNOWN SOLITAIRE
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·December 21, 2023