
Globus Medical, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO BEACON STABILIZATION SYSTEM is an FDA 510(k)-cleared medical device (K092610) manufactured by Globus Medical, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 23, 2009. Regulation: 8.