GAIA Lumbar Interbody Fusion Device (LIFD) Family

GAIA Lumbar Interbody Fusion Device (LIFD) Family is an FDA 510(k)-cleared medical device (K201939) manufactured by Printerprezz. 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 7, 2020. Regulation: 8.