Life Spine Gains Additional FDA 510(k) for Lateral PROLIFT Expandable System

By Julie A. Vetalice

Life Spine Gains Additional FDA 510(k) for Lateral PROLIFT Expandable System

Life Spine received an additional 510(k) clearance from FDA to market the Lateral PROLIFT Expandable System. Further, the company plans to launch 20 new products in 2020, including six Micro Invasive Expandables.

Life Spine’s expandable portfolio includes:

  • Lateral PROLIFT Expandable System
  • 10mm and 12mm PROLIFT Expandable Systems for TLIF and PLIF approaches
  • AILERON® TRX Expandable Interspinous Spacer
  • LONGBOW® Expandable Lateral Spacer System
  • LONGBOW Expandable TLIF Spacer System
  • TiBOW™ Expandable Spacer System with horizontal expansion for a TLIF approach

“This year we will add some pivotal new technologies to our already robust expandable portfolio bringing our total number of expandable devices to 13,” said Rich Mueller, Chief Operating Officer for Life Spine. “Investing in expandable technologies is important to us because expandables are designed to allow for a truly Micro Invasive procedure by going in small and opening to match each patient’s unique anatomy. Our dedication to offering expandable solutions dates back to 2006 when we filed our first patent around expandable technology and now we aim to file one patent each month.”

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory