Iconix Knotless Anchor
K-Number: K243323 · 2024-11-19
ApplicantRiverpoint Medical
Decision Date2024-11-19
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Iconix Knotless Anchor is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2024-11-19 under approval number K243323. 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 Knotless Anchor?
Iconix Knotless Anchor is a medical device that received FDA 510(k) clearance on 2024-11-19. It is manufactured by Riverpoint Medical. The 510(k) number is K243323.
When was Iconix Knotless Anchor approved by the FDA?
Iconix Knotless Anchor received FDA 510(k) clearance on 2024-11-19, under approval number K243323.
What company makes Iconix Knotless Anchor?
Iconix Knotless Anchor is manufactured by Riverpoint Medical.
What is the FDA product code for Iconix Knotless Anchor?
The FDA product code for Iconix Knotless 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.