MEQUON, Wis.--(BUSINESS WIRE)--Titan Spine, LLC announced today that it began limited market release of its ENDOSKELETON® TT system, a new transforaminal lumbar interbody fusion (TLIF) device. The ENDOSKELETON® TT received 510(k) clearance from the U.S. Food and Drug Administration April 15, 2009. This represents the second clearance and product for Titan Spine as the company builds its portfolio of bioactive spinal devices.
