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FDA 510(k)

Aventus Thrombectomy System (IM-2001/IM-0002)

K-Number: K240117 · 2024-03-15

Decision Date2024-03-15
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aventus Thrombectomy System (IM-2001/IM-0002) is a medical device manufactured by Inquis Medical. It received FDA 510(k) clearance on 2024-03-15 under approval number K240117. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aventus Thrombectomy System (IM-2001/IM-0002)?

Aventus Thrombectomy System (IM-2001/IM-0002) is a medical device that received FDA 510(k) clearance on 2024-03-15. It is manufactured by Inquis Medical. The 510(k) number is K240117.

When was Aventus Thrombectomy System (IM-2001/IM-0002) approved by the FDA?

Aventus Thrombectomy System (IM-2001/IM-0002) received FDA 510(k) clearance on 2024-03-15, under approval number K240117.

What company makes Aventus Thrombectomy System (IM-2001/IM-0002)?

Aventus Thrombectomy System (IM-2001/IM-0002) is manufactured by Inquis Medical.

What is the FDA product code for Aventus Thrombectomy System (IM-2001/IM-0002)?

The FDA product code for Aventus Thrombectomy System (IM-2001/IM-0002) is QEW.

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Official Source

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