Custom Spine’s PATHWAY ACIF Gets FDA Clearance

Custom Spine of Parsippany, NJ has received FDA clearance to market PATHWAY ACIF, an anterior cervical interbody spacer. Available in 0° parallel and 7° lordotic profiles and a range of heights from 5mm to 12mm, the radiolucent spacer features a large footprint to enhance structural support and a large graft window to promote bone fusion. The device complements the company’s low-profile anterior cervical plate system Regent ACP released last November, and is intended for use in spinal fusion procedures at one level (C2-T1) in skeletally mature patients with degenerative disc disease.
Product page: PATHWAY ACIF…
Press Release: Custom Spine Receives FDA Clearance for PATHWAY ACIF…