PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM

PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM is an FDA 510(k)-cleared medical device (K974203) manufactured by Integrated Orbital Implants, 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 February 3, 1998. Regulation: 8.