Life Spine announced that it won FDA 510(k) clearance for its steerable Plateau Ti system for surface treatment for potential bone growth.
Plateau Ti is a titanium interbody system designed to provide an optimal environment for bone growth in both transforaminal lumbar interbody fusion (TLIF) and posterior lumbar interbody fusion (PLIF). It is used to facilitate controlled delivery upon insertion to facilitate positioning in the anterior portion of the disc space.
The system features a curved design to match patient anatomy and maximize endplate coverage. It also includes the Osseo-Loc surface treatment, a simplified insertion process and large, open graft windows. It is available in lengths of 28mm and 32mm with heights ranging from 9mm to 14mm in 1mm increments.
“The steerable Plateau Ti System is one of many novel systems slated to join our micro-invasive portfolio this year,” Life Spine president & CEO Michael Butler said in a news release. “These launches are testimony to our continued dedication in supporting less invasive procedures.”