Triathlon Tritanium Central Femoral Cone Augment, Triathlon Femoral Distal Augment

Triathlon Tritanium Central Femoral Cone Augment, Triathlon Femoral Distal Augment is an FDA 510(k)-cleared medical device (K190991) manufactured by Howmedica Osteonics Corp. (Aka Stryker Orthopaedics). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 14, 2019. Regulation: 8.