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.
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
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