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AXS Vecta Aspiration Catheter

by Stryker Neurovascular

510(k) K190833

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

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 NumberK190833 Date15 Dec 2019ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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

From the manufacturer

Engineered with versatility in mind, the AXS Vecta 46 Intermediate Catheter is designed to take support farther in hemorrhagic procedures, give you options to effectively treat distal occlusions, and provide delivery support for your large bore catheters—all in one simple platform.

Source: stryker.com

That's why we're introducing the AXS Vecta Intermediate Catheter. Upgraded with Pro Technology, this catheter's extra-large lumen is designed for powerful clot removal through aspiration alone or with a stent retriever. Together, with our customers, we are driven to make healthcare better.

Source: stryker.com

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