8 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES TITANIUM (TI) ALLOY HIGH TIBIAL OSTEOTOMY (HTO) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·February 6, 2017
SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295246176·SIGMA TC3 RP INSERT TRIAL SIZE 2 20mm
FLEXIFLO (R) VERSA-PEG (TM) GASTROSTOMY KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE
FDA 510(k)
FDA Class 2
·Radiology
PLUM A+ DRIVER NEW 8
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 19, 2014
2520274-2013-10027
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 13, 2013
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·January 14, 2011