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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 the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2019-12-15 under 510(k) 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. The listed applicant is Stryker Neurovascular. The 510(k) number is K190833.

When did AXS Vecta Aspiration Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for AXS Vecta Aspiration Catheter?

The FDA 510(k) record lists Stryker Neurovascular as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Clinical Trials

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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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