TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE

TITAN MERIDIAN INTERSEGMENTAL ROLLERTABLE is an FDA 510(k)-cleared medical device (K905756) manufactured by Titan Technology Intl., Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 7, 1991. Regulation: 8.