Peekplus® Interbody Fusion Device

Peekplus® Interbody Fusion Device is an FDA 510(k)-cleared medical device (K173864) manufactured by Vallum Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 1, 2018. Regulation: 8.