7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EXETER MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RESPONSE(TM) STEERABLE CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
TYPE 9210 S/ECG
FDA 510(k)
FDA Class 2
·Cardiovascular
SENSIA
FDA Adverse Event
Death
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·February 15, 2013
SM104 MSERIES W5TH WHL
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIVISION·Product code FPO·January 12, 2011
EMAX 2 MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 13, 2013
ANKLE LOCKING NAIL 10 X 150MM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code HSB·May 28, 2019