510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K212057Substantially Equivalent

Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS

Artventive Medical Group, Inc., San Marcos CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K212057 is the FDA 510(k) clearance record for Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS, a class II device, cleared for Artventive Medical Group, Inc. on under FDA product code KRD (Device, Vascular, For Promoting Embolization). FDA records list 3 510(k) clearances for Artventive Medical Group, Inc., from to . As of , FDA records show no recalls naming K212057.

Clearance record

Decision date
Received
(243 days to decision)
Product code
KRD Device, Vascular, For Promoting Embolization
Regulation
21 CFR 870.3300
Device class
Class II
Review panel
Cardiovascular
Applicant
Artventive Medical Group, Inc. 1797 Playa Vista, San Marcos CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KRD

Trailing 12 months
7 clearances under product code KRD in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KRD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20261
May 20260
June 20262
July 20262
August 20260
September 20260
October 20260