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
Vice-President of Technology and Regulatory Affairs
AdvaMed
Washington DC, DC
Sr Product Manager Global Marketing (US/DA/00/0085/SL) - 14000009V3
Abbott
Chicago, IL
Director of Medicare Products
Bluegrass Family Health
Lexington, KY
Director of Medicare Products
Bluegrass Family Health
Lexington, KY
Vice President, Information Technology
HealthPartners
MN