Orthofix International N.V. announced U.S. Food and Drug Administration (FDA) and European CE Mark approvals for its next-generation CervicalStim™ and SpinalStim™ bone growth stimulators. These Class III medical devices use a low-level pulsed electromagnetic field (PEMF) designed to activate and augment the body's natural healing process, providing patients with a safe, noninvasive treatment option for promoting post-operative spinal fusion.