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FDA 510(k)

AXS Vecta Aspiration Catheter

K-Number: K190833 · 2019-12-15

ApplicantStryker Neurovascular
Decision Date2019-12-15
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AXS Vecta Aspiration Catheter is a medical device manufactured by Stryker Neurovascular. It received FDA 510(k) clearance on 2019-12-15 under approval number K190833. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXS Vecta Aspiration Catheter?

AXS Vecta Aspiration Catheter is a medical device that received FDA 510(k) clearance on 2019-12-15. It is manufactured by Stryker Neurovascular. The 510(k) number is K190833.

When was AXS Vecta Aspiration Catheter approved by the FDA?

AXS Vecta Aspiration Catheter received FDA 510(k) clearance on 2019-12-15, under approval number K190833.

What company makes AXS Vecta Aspiration Catheter?

AXS Vecta Aspiration Catheter is manufactured by Stryker Neurovascular.

What is the FDA product code for AXS Vecta Aspiration Catheter?

The FDA product code for AXS Vecta Aspiration Catheter is DQY.

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Related Devices (Code: DQY)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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