510(k) K261363

Y-Knotless™ Flex Anchors by CONMED Corporation — Product Code MBI

K261363 is an FDA 510(k) premarket notification submitted by CONMED Corporation for the device "Y-Knotless™ Flex Anchors". The FDA issued a decision of Substantially Equivalent on May 13, 2026. The device falls under product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue), a Class II device regulated under 21 CFR 888.3040. CONMED Corporation has at least 10 other 510(k) clearances on record.