Iconix® Anchor
K-Number: K241577 · 2024-07-03
ApplicantRiverpoint Medical
Decision Date2024-07-03
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 2024-07-03 under approval number K241577. 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 2024-07-03. It is manufactured by Riverpoint Medical. The 510(k) number is K241577.
When was Iconix® Anchor approved by the FDA?
Iconix® Anchor received FDA 510(k) clearance on 2024-07-03, under approval number K241577.
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.