KNOXVILLE, TN, June 7, 2015 – ChoiceSpine, a Knoxville, TN based spinal implant company, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market titanium lumbar interbody fusion devices. ChoiceSpine plans to offer titanium interbody devices for traditional PLIF (Posterior Lumbar Interbody Fusion) and TLIF (Transforaminal Lumbar Interbody Fusion) approaches as well as the new VLIF (Visualized Lateral Interbody Fusion) approach.
If you would like more information about ChoiceSpine’s titanium offering please email [email protected]
About ChoiceSpine
ChoiceSpine is a privately held spine company located in Knoxville, TN, and prides itself on providing excellent products and exceptional service to meet the needs of their customers. ChoiceSpine offers a breadth of innovative and surgeon focused systems that are designed to be safe, efficient, and easy-to-use.