NLT Spine Receives FDA Clearance for Second Generation Spine Fusion Devices

Written by Heather Linder | November 12, 2013 | Print  |

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.

More Articles on Devices:

Lawnwood Regional Medical Center Purchases Mazor Robotics' Renaissance Spine System
Titan Spine Celebrates 18k Implantations of Interbody Fusion Device
Spinal Devices Supplied by Physician-Owned Distributors: Overview of Prevalence and Use, Report by Daniel Levinson, OIG DHHS — 10 Key Points and Observations

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