NLT SPINE Receives 510(k) Clearance for its Lumbar Interbody Fusion Device, PROW FUSION™
2/1/2012 8:43:15 AM
KFAR SABA, Israel--(BUSINESS WIRE)--NLT SPINE, a developer of Minimally Invasive Spine Surgery (MISS) products, today announced that its PROW FUSION™ device received 510(k) clearance from the U.S. Food and Drug Administration (FDA).
NLT SPINE’s PROW FUSION™ Transforaminal-Lumbar Interbody Fusion (TLIF) device and delivery system are intended for spinal fusion in TLIF procedures. The product was developed based on NLT SPINE's non-linear core technology which allows for inserting large implants and instruments through a small incision. NLT SPINE’s non-linear core technology was invented by Dr. Tzony Siegal.