SeaSpine Ventura NanoMetalene System

SeaSpine Ventura NanoMetalene System is an FDA 510(k)-cleared medical device (K173022) manufactured by SeaSpine Orthopedics 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 October 25, 2017. Regulation: 8.