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NLT Spine Receives FDA Approval for Second Generation PROW FUSION and eSPIN Spinal Devices

November 12th, 2013 Gaurav Orthopedic Surgery

PROW-FUSIONNLT Spine (Kfar Saba, Israel), a maker of minimally invasive spinal technologies, has received FDA approval for the second generation  of the PROW FUSION implant and eSPIN discectomy tool. The two devices help to perform  lumbar interbody fusion via a small posterior incision in a reliable, safe and minimally invasive procedure. The second generation products make use of fewer instruments, better irrigation, improved material and optimized design.

The PROW FUSION interbody fusion implant, which is used for Transforaminal Lumbar Interbody Fusion (TLIF) procedures, consists of a segmented non-linear structure that is implanted in a straight configuration using a protective conduit. The conduit is pre-inserted using a keyhole incision. When  the implant reaches the  intervertebral space it takes up a circular form thereby forming a footprint larger than competing technologies. This larger footprint results in larger bone graft volume within the implant.

The eSPIN Discectomy System is used during discectomy for fusion procedures in L2-S1 spinal segments in order to cut and grind intervertebral disc material. The system comes with single use cutting tips, a hand-held instrument, a motor adaptor and a range of access and positioning instruments. Use of the eSPIN system results in removal of 67% more disc volume compared to competing procedures, and 83% fewer passes of the instrument near the exiting nerve. The eSPIN and PROW FUSION systems are designed to be used during minimally invasive spine surgery with spinal fixation systems such as posterior pedicle screw and rod systems.

Press release: NLT SPINE’s PROW FUSION™ and eSPIN™ Receive 510(k) Clearance…

Product pages: PROW FUSION…; eSPIN…

Gaurav

Gaurav Krishnamurthy, PhD is a Senior R&D engineer at a Bay Area based medical device start-up. Gaurav has a strong passion for medical device innovation and is interested in disruptive medical technologies that not only solve an unmet clinical need, but also bring down the cost of healthcare. Gaurav closely follows medical device trends in emerging markets and is fascinated by simple and inexpensive solutions to major healthcare problems. Gaurav earned his PhD and Master's in Mechanical Engineering from Stanford University where he developed state of the art computational models of beating heart valves that can be used to design and test heart valve prosthetics. Gaurav was a Medtronic BioX Fellow at Stanford University. Gaurav also serves as a Senior Advisor to a Bay Area angel investment group focusing on mobile health and healthcare innovation.

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