Titan Spine Receives FDA 510(k) Clearance on PLIF Device

Titan Spine, a Mequon, Wis.-based spinal fusion implant developer, received FDA clearance for its Endoskeleton TO system for posterior lumbar interbody fusion, according to a company news release.

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The Endoskeleton TO device includes a roughened titanium surface that helps during in the fusion process. The device was designed to promote earlier bone in-growth and stability.

Read the Titan Spine release on Endoskeleton TO.

Read other coverage on spine devices:

– Wenzel Spine Receives FDA Clearance on Spinal System

– ArthroCare Receives FDA Clearance for Vertebral Augmentation Device

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