LDR's device to reduce need for thick cervical plates gets FDA OK

04/25/2012 | BeckersOrthopedicAndSpine.com

The FDA has granted LDR 510(k) clearance to market its ROI-C Lordotic Cervical Cage, which works with the spinal device firm's VerteBRIDGE plating system. The device is designed to limit the use of thick cervical plates, which may cause dysphagia.

View Full Article in:


Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Eastern Zone Sales Director
Regenesis Biomedical
Multiple Locations, SL_Multiple Locations
Director, Compliance - Health Plan Privacy & Security
Kaiser Permanente
Oakland, CA
Regulatory Counsel
Food and Drug Administration
Silver Spring, MD
Pharmacy Care Manager
National Association of Chain Drug Stores
Arlington, VA
Vice President, Commercial Markets
Meridian Health
Neptune, NJ