NLT Spine Receives FDA Clearance for Second Generation Spine Fusion Devices

NLT Spine received FDA 510(k) approval for its second generation PROW FUSION implant and eSPIN discectomy tool, according to a Med Gadget report. The devices are for lumbar interbody fusions through a minimally invasive posterior incision. The next generation of the device uses fewer instruments and improved materials.

The PROW FUSION is for TLIF procedures and the eSPIN Discectomy System for discectomy in the L2-S1 spinal segments.

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