510(k) K253713

Arthrex Variable Angle (VA) Proximal Tibia Plating System by Arthrex, Inc. — Product Code HRS

K253713 is an FDA 510(k) premarket notification submitted by Arthrex, Inc. for the device "Arthrex Variable Angle (VA) Proximal Tibia Plating System". The FDA issued a decision of Substantially Equivalent on January 21, 2026. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Arthrex, Inc. has at least 10 other 510(k) clearances on record.