US FDA clears Life Spine's minimally-invasive surgery equipment
This article was originally published in Clinica
Executive Summary
Life Spine's FS3 spinal system has gained 510(k) clearance from the US FDA. The system is composed of cannulated, wire-guided, minimally-invasive implants and instrumentation, which can be used for both percutaneous and open surgery. The FS3 will be launched in the US in August, the Hoffman Estates, Illinois company said.