Kneevoice Cartilage Evaluation System (750-3600-001)

Kneevoice Cartilage Evaluation System (750-3600-001) is an FDA 510(k)-cleared medical device (K252076) manufactured by Kneevoice, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 5, 2026. Regulation: 8.