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FDA 510(k) K133924, ENDOLUMINAL OCCLUSION SYSTEM (EOS), by Artventive Medical Group, Inc.

FDA 510(k) K133924, ENDOLUMINAL OCCLUSION SYSTEM (EOS), by Artventive Medical Group, Inc.

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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
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