Hive™ Stand-alone Anterior Lumbar Interbody System

Hive™ Stand-alone Anterior Lumbar Interbody System is an FDA 510(k)-cleared medical device (K200541) manufactured by Hd Lifesciences, 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 April 27, 2020. Regulation: 8.