The U.S. Food and Drug Administration (FDA) has granted 510 (k) clearance to an expandable lateral lumbar interbody system.

Without Shawn Collins, a Chicago attorney, the North American Spine Society would not likely exist, and the development of ...

Titan Spine, LLC recently announced that it has received 510(k) clearance from the FDA to market its Endoskeleton line of interbody fusion implants featuring its next generation nanoLOCK surface ...