




Healthcare Industry News: Titan Spine
News Release - October 4, 2010
Titan Spine Launches Alternative Bioactive Cervical Device
MEQUON, Wis.--(Healthcare Sales & Marketing Network)-- Titan Spine announced that it will begin full commercial release of its new Endoskeleton® TC system first quarter of 2011. The Endoskeleton® TC is an interbody fusion device for the cervical spine. The product received 510(k) clearance in July of this year and has been in limited market release since early August. The device has an acid etched titanium surface and is biomechanically designed to promote spinal fusion.This represents the third regulatory clearance for Titan Spine as the company continues to build its portfolio of bioactive spinal interbody fusion devices. “The design and technology utilized cater to the biology of healing,” stated Jennifer Schneider, Sr. Research and Development Engineer. “Titan Spine is pleased to offer a device that presents unique benefits to providing treatment for patients with degenerative disc disease in the cervical spine.”
Surgeons are excited to learn about the bony ingrowth benefits the Endoskeleton® TC provides especially at a time when the use of BMP and plastic devices are under scrutiny.
About Titan Spine - Titan Spine, LLC is a privately owned company in Mequon, Wisconsin focusing on the design and manufacturing of bioactive interbody fusion devices for the spine. Founded in 2005, the company is committed to developing advanced products for treatment of various pathologies that cause back pain.
Source: Titan Spine
Issuer of this News Release is solely responsible for its
content.
Please address inquiries directly to the issuing company.