FDA 510(k), K133924, ENDOLUMINAL OCCLUSION SYSTEM (EOS)

510(K) Number: K133924
Device Name: ENDOLUMINAL OCCLUSION SYSTEM (EOS)
Manufacturer: ARTVENTIVE MEDICAL GROUP, INC
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/23/2013
Decision Date: 12/03/2014
Regulation Medical Specialty: Cardiovascular

Total pages: 1156
Fully redacted pages: 720
Content pages: 436