Iconix Anchor
K-Number: K233468 · 2023-11-14
ApplicantRiverpoint Medical
Decision Date2023-11-14
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Iconix Anchor is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2023-11-14 under approval number K233468. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Iconix Anchor?
Iconix Anchor is a medical device that received FDA 510(k) clearance on 2023-11-14. It is manufactured by Riverpoint Medical. The 510(k) number is K233468.
When was Iconix Anchor approved by the FDA?
Iconix Anchor received FDA 510(k) clearance on 2023-11-14, under approval number K233468.
What company makes Iconix Anchor?
Iconix Anchor is manufactured by Riverpoint Medical.
What is the FDA product code for Iconix Anchor?
The FDA product code for Iconix Anchor is MBI.
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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.