Orthofix devices obtain approvals in the U.S., Japan

09/9/2008 | Pharmaceutical Business Review Online

The FDA has given 510(k) clearance to Orthofix International's Pillar SA spine interbody device, which is designed to eliminate the need for supplemental internal fixation during lumbar spinal fusion surgeries. The company also secured approval in Japan for its CentroNail line of nailing systems that are used for stabilizing leg bone fractures.

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