Life Spine Announces FDA 510(k) Clearance for the PLATEAU-A Ti Anterior Lumbar Spacer System

By Julie A. Vetalice

Life Spine Announces FDA 510(k) Clearance for the PLATEAU-A Ti Anterior Lumbar Spacer System

Life Spine received FDA 510(k) clearance to market the PLATEAU-A Ti Anterior Lumbar spinal spacer.

PLATEAU-A Ti can be used for anterior spinal fusion. Multiple footprint sizes and various heights accommodate patient anatomies and pathologies to promote fusion.

The device features large, open graft windows allow maximum visibility and bone graft containment, Osseo-Loc™ surface treatment technology to promote bony ongrowth, and a chamfered leading edge to ease implant insertion.

“With the increased usage of anterior column reconstruction, PLATEAU-A Ti fills an important portfolio gap. Joining our recently launched DYNA-LINK® Titanium Stand-Alone ALIF Spacer System and SENTRY® ALIF Plating System, this clearance expands our robust ALIF portfolio,” said Rich Mueller, Chief Operating Officer for Life Spine. “Continuing our success with previous interbody technologies, PLATEAU-A Ti provides surgeons with a titanium implant available in a variety of heights, widths, and lordotic options.”

Product Labels: Lumbar Spine, Spinal Fusion

Tags: 510(k) Clearance, Regulatory