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Merit Siege Vascular Plug

by Merit Medical System, Inc.

510(k) K212817

Merit Siege Vascular Plug is a Class II device made by Merit Medical System, Inc., cleared under FDA 510(k) K212817 on 15 Dec 2021, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK212817 Date15 Dec 2021ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
KRD
Device class
Class II
Regulation
21 CFR Part 870.3300
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code KRD (Device, Vascular, For Promoting Embolization).

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