Y-Knotless Flex Anchors
K-Number: K253763 · 2026-01-29
ApplicantConmed Corporation
Decision Date2026-01-29
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Y-Knotless Flex Anchors is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2026-01-29 under approval number K253763. 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 Y-Knotless Flex Anchors?
Y-Knotless Flex Anchors is a medical device that received FDA 510(k) clearance on 2026-01-29. It is manufactured by Conmed Corporation. The 510(k) number is K253763.
When was Y-Knotless Flex Anchors approved by the FDA?
Y-Knotless Flex Anchors received FDA 510(k) clearance on 2026-01-29, under approval number K253763.
What company makes Y-Knotless Flex Anchors?
Y-Knotless Flex Anchors is manufactured by Conmed Corporation.
What is the FDA product code for Y-Knotless Flex Anchors?
The FDA product code for Y-Knotless Flex Anchors 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.