CRANIAL SYMMETRY SYSTEM

CRANIAL SYMMETRY SYSTEM is an FDA 510(k)-cleared medical device (K022273) manufactured by Beverly Hills Prosthetics Orthotics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 8, 2002. Regulation: 8.