The procedure was performed by Jess Lonner, MD, at the Thomas Jefferson Riverview Surgical Center in Philadelphia. Dr. Lonner is also an attending orthopedic surgeon at Rothman Institute in Philadelphia.
The Navio system received a CE Mark in the first quarter of 2012. In December 2012, the U.S. FDA granted the device 510(k) approval to sell and market it in the country.
More Articles on Supply Chain:
Device Companies — 7 Key Notes — Biomet, MAKO Surgical & More
Victrex Group Finance Director Steve Barrow to Step Down
Study Shows SpineJack Device Effective for Vertebral Compression Fracture Treatment
