US FDA clears Life Spine's minimally-invasive surgery equipment
This article was originally published in Clinica
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.
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