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.

View Full Article in:

Pharmaceutical Business Review Online

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Senior Director Medical Affairs
Edwards Lifesciences
Irvine, CA
Senior Scientist - Cell Engineering Group
Pfizer
San Francisco, CA
Medical Director - Physician
Willamette Valley Community Health
Salem, OR
Area Reimbursement Manager (CT, MA, MD, ME, NH, NJ, NY, PA, VT)
SI-BONE, INC
Multiple Locations, SL_Multiple Locations
Medical Director - Physician
Willamette Valley Community Health
Salem, OR