6 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TIBIAL INSERT
FDA 510(k)
FDA Class 2
·Orthopedic
Medline ReNewal Reprocessed Stryker External Fixation Devices
FDA 510(k)
FDA Class 2
·Orthopedic
VECTORVISION HIP SR
FDA 510(k)
FDA Class 2
·Neurology
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2014
PIN COLLET
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code HRX·January 24, 2013
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code LXH·January 18, 2011