Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices

Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices is an FDA 510(k)-cleared medical device (K223065) manufactured by Adcura, 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, 2022. Regulation: 8.