6 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CODMAN SOF'WIRE TITANIUM CABLE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
'RAPIDTEC'-5M-MULTIPLE DIP TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
1.8MM TI LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code KWQ·January 22, 2013
AML STD 15.0MM 6.3 IN STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LZO·December 8, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 9, 2014