Artix MT; Artix Thin-Walled Thrombectomy Sheath
K-Number: K241894 · 2024-10-15
ApplicantInari Medical, Inc.
Decision Date2024-10-15
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Artix MT; Artix Thin-Walled Thrombectomy Sheath is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2024-10-15 under approval number K241894. 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 Artix MT; Artix Thin-Walled Thrombectomy Sheath?
Artix MT; Artix Thin-Walled Thrombectomy Sheath is a medical device that received FDA 510(k) clearance on 2024-10-15. It is manufactured by Inari Medical, Inc.. The 510(k) number is K241894.
When was Artix MT; Artix Thin-Walled Thrombectomy Sheath approved by the FDA?
Artix MT; Artix Thin-Walled Thrombectomy Sheath received FDA 510(k) clearance on 2024-10-15, under approval number K241894.
What company makes Artix MT; Artix Thin-Walled Thrombectomy Sheath?
Artix MT; Artix Thin-Walled Thrombectomy Sheath is manufactured by Inari Medical, Inc..
What is the FDA product code for Artix MT; Artix Thin-Walled Thrombectomy Sheath?
The FDA product code for Artix MT; Artix Thin-Walled Thrombectomy Sheath is QEW.
Related Clinical Trials
Other Devices by Inari Medical, Inc.
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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.