Lumbar Expandable lnterbody Spacers -Additional Indications/Implants

Lumbar Expandable lnterbody Spacers -Additional Indications/Implants is an FDA 510(k)-cleared medical device (K221894) manufactured by Globus Medical, 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 August 2, 2023. Regulation: 8.