Tomier Perform™ Reversed Glenoid Cannulated Glenospheres

Tomier Perform™ Reversed Glenoid Cannulated Glenospheres is an FDA 510(k)-cleared medical device (K213124) manufactured by Tornier, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 25, 2021. Regulation: 8.