-

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

HUNTLEY, Ill.--(BUSINESS WIRE)--Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market the PLATEAU-A Ti Anterior Lumbar Spacer System.

“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.”

PLATEAU-A Ti Anterior Lumbar Spacer System is a comprehensive system that can be used for anterior fusion procedures. Multiple footprint sizes are available in various heights to accommodate individual patient anatomies and pathologies to promote fusion.

Key Features and Benefits:

  • Large, open graft windows for maximum visibility and bone graft containment
  • Osseo-Loc™ Surface Treatment Technology
  • Chamfered leading edge to ease implant insertion

About Life Spine

Life Spine is dedicated to improving the quality of life for spinal patients by increasing procedural efficiency and efficacy through innovative design, uncompromising quality standards, and the most technologically advanced manufacturing platforms. Life Spine, which is privately held, is based in Huntley, Illinois. For more information, please visit: http://www.lifespine.com and/or https://www.micro-invasive.com.

Contacts

Mr. Omar Faruqi
Chief Financial Officer
ofaruqi@lifespine.com
847-884-6117

Industry:

Life Spine

Release Versions
English

Contacts

Mr. Omar Faruqi
Chief Financial Officer
ofaruqi@lifespine.com
847-884-6117

More News From Life Spine

Life Spine Receives FDA 510(k) Clearance for VersaLift™ Expandable Interbody System Featuring a 6mm Starting Height

HUNTLEY, Ill.--(BUSINESS WIRE)--Life Spine, Inc., a medical device company that designs, develops, manufactures, and markets products for the surgical treatment of spinal disorders, announced today that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the VersaLift™ Expandable Interbody System, a Micro Invasive™ solution for TLIF and PLIF procedures featuring a low 6mm starting height. Designed to support minimally invasive surgical access, VersaLift offers one of th...

Life Spine Announces “Total Victory” in Patent Battle with Globus

HUNTLEY, Ill.--(BUSINESS WIRE)--Today the United States Court of Appeals, Federal Circuit, issued an opinion rejecting Globus’s last-remaining patent claim against Life Spine. In 2021, Globus sued Life Spine alleging that Life Spine’s ProLift® line of products infringed Globus patents. Life Spine challenged the patentability of several of the patents and, in 2024, the United States Patent Trial & Appeal Board cancelled all of the claims from four patents that Globus had asserted against Lif...

Life Spine Announces Expanded Indications for ARx® SAI Spinal Fixation System

HUNTLEY, Ill.--(BUSINESS WIRE)--Life Spine, Inc., a medical device company that designs, develops, manufactures, and markets products for the surgical treatment of spinal disorders, announced today their 510k for ARx SAI (Sacral Alar Iliac) Spinal Fixation System was approved. ARx SAI has expanded its compatibility clearance and is now approved for use with compatible pedicle screws with 5.5mm or 6.0mm posterior rods made from either titanium alloys or cobalt chrome, including those from compet...
Back to Newsroom