Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System

Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System is an FDA 510(k)-cleared medical device (K200328) manufactured by Kyocera Medical Technologies, 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 March 10, 2020. Regulation: 8.