Triever20 Curve (21-201)
K-Number: K231848 · 2023-07-21
ApplicantInari Medical, Inc.
Decision Date2023-07-21
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Triever20 Curve (21-201) is a medical device manufactured by Inari Medical, Inc.. It received FDA 510(k) clearance on 2023-07-21 under approval number K231848. 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 Triever20 Curve (21-201)?
Triever20 Curve (21-201) is a medical device that received FDA 510(k) clearance on 2023-07-21. It is manufactured by Inari Medical, Inc.. The 510(k) number is K231848.
When was Triever20 Curve (21-201) approved by the FDA?
Triever20 Curve (21-201) received FDA 510(k) clearance on 2023-07-21, under approval number K231848.
What company makes Triever20 Curve (21-201)?
Triever20 Curve (21-201) is manufactured by Inari Medical, Inc..
What is the FDA product code for Triever20 Curve (21-201)?
The FDA product code for Triever20 Curve (21-201) is 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.