Biomet Microfixation Thoracic Fixation System

Biomet Microfixation Thoracic Fixation System is an FDA 510(k)-cleared medical device (K142823) manufactured by Biomet Microfixation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 24, 2015. Regulation: 8.