Y-Knotless Flex Anchors
K-Number: K261363 · 2026-05-13
ApplicantCONMED Corporation
Decision Date2026-05-13
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 2026-05-13 under approval number K261363. 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 2026-05-13. It is manufactured by CONMED Corporation. The 510(k) number is K261363.
When was Y-Knotless Flex Anchors approved by the FDA?
Y-Knotless Flex Anchors received FDA 510(k) clearance on 2026-05-13, under approval number K261363.
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.
Related Devices (Code: MBI)
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.