MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT

MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT is an FDA 510(k)-cleared medical device (K941717) manufactured by Miguel Martinez M.D.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 13, 1995. Regulation: 8.