7 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Hi-Dow Wireless TENS/EMS System (Model HD-5N)
FDA 510(k)
FDA Class 2
·Neurology
POLARIS SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SMALL STATURE SPACERS
FDA 510(k)
FDA Class 2
·Orthopedic
4.0MM TI LOCKING SCREW W/T25 STARDRIVE 26MM F/IM NAILS-STER
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·March 20, 2018
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013
VENTAK PRIZM 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 15, 2011
COONRAD/MORREY TOTAL ELBOW INTERCHANGEABLE HUMERAL ASSEMBLY
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code JDC·September 10, 2008