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Barricade Embolization Coil System

by Blockade Medical 510(k)

Active United States

510(k) K151760

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK151760 Date27 Jul 2015ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
HCG
Device Class
Class II
Regulation
21 CFR Part 882.5950
Advisory Committee
Neurology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Barricade Embolization Coil System is a neurovascular embolization device designed to occlude blood vessels. It employs coils to induce clot formation, effectively blocking abnormal blood flow in conditions such as aneurysms or arteriovenous malformations (AVMs).

This system is delivered via a catheter and deployed endovascularly, allowing precise positioning within cerebral vasculature. It is supplied as a sterile, single-use device and falls under FDA 510(k) clearance (K151760) as a Class II medical device (product code HCG). The coils are available in multiple configurations, including framing and helical designs, with sizes ranging from 2 mm to 15 mm.

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