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Mindframe Capture LP Revascularization Device

by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular

510(k) K141516

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK141516 Date5 Feb 2015ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-1701-2018 FDA Class I initiated 26 Feb 2018

    There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery wire.

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  • Withdrawn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
NRY
Device Class
Class II
Regulation
21 CFR Part 870.1250
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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