ClotTriever XL Catheter
K-Number: K223210 · 2023-04-27
ApplicantInari Medical, Inc.
Decision Date2023-04-27
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
ClotTriever XL Catheter is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2023-04-27 under approval number K223210. 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 ClotTriever XL Catheter?
ClotTriever XL Catheter is a medical device that received FDA 510(k) clearance on 2023-04-27. It is manufactured by Inari Medical, Inc.. The 510(k) number is K223210.
When was ClotTriever XL Catheter approved by the FDA?
ClotTriever XL Catheter received FDA 510(k) clearance on 2023-04-27, under approval number K223210.
What company makes ClotTriever XL Catheter?
ClotTriever XL Catheter is manufactured by Inari Medical, Inc..
What is the FDA product code for ClotTriever XL Catheter?
The FDA product code for ClotTriever XL Catheter is QEW.
Other Devices by Inari Medical, Inc.
Related Devices (Code: QEW)
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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.