Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System

K260102 is the FDA 510(k) clearance record for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System, a class II device, cleared for Stryker Corporation (Tornier, Inc.) on 2026-06-12 under FDA product code PHX (Shoulder Prosthesis, Reverse Configuration). FDA's definition for product code PHX reads: "Intended to be used to relieve pain and to replace the glenoid and humeral side of the shoulder joint in order to restore mobility in a grossly rotator cuff deficient joint with severe arthropathy or a previous joint replacement with a...". FDA records list 3 510(k) clearances for Stryker Corporation (Tornier, Inc.), from 2024-09-10 to 2026-06-12. As of 2026-09-10, FDA records show no recalls naming K260102.