Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System

Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System is an FDA 510(k)-cleared medical device (K220413) manufactured by Canary Medical USA, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 21, 2022. Regulation: 8.