MEDPOR QUAD MOTILITY IMPLANT

MEDPOR QUAD MOTILITY IMPLANT is an FDA 510(k)-cleared medical device (K010902) manufactured by Porex Surgical, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 18, 2001. Regulation: 8.