TITANIUM PEG SYSTEM

TITANIUM PEG SYSTEM is an FDA 510(k)-cleared medical device (K980822) manufactured by Fci Ophthalmics, 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 July 8, 1998. Regulation: 8.