June 18, 2019 HUNTLEY, Ill.–(BUSINESS WIRE)–Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that the Food and Drug Administration has provided 510(k) market clearance for the PROLIFT Lateral Expandable Spacer System. “The PROLIFT Lateral Expandable Spacer System is a significant addition …