Aventus Thrombectomy System (IM-2001/IM-0002)
K-Number: K240117 · 2024-03-15
Device Summary
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.
Related Clinical Trials
Other Devices by Inquis Medical
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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.