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Interventional Spine Receives FDA Clearance for Spine Device

Written by  Laura Miller | January 26, 2012
Interventional Spine, an Irvine, Calif.-based spine device company, has received FDA clearance for its Opticage Expandable Intervertebral Body Fusion device, according to a company news release.
The Opticage is part of Interventional Spine's PerX360 System and can be used with the Optiport Access Instrument. The system is now the only system designed for surgeons to perform a complete percutaneous lumbar interbody fusion with two 15-mm incisions for treating lumbar discogenic pain.

Related Articles on Spine Devices:

Life Spine Reports 29% Revenue Growth in 2011

Choice Spine Launches Starfire Pedicle Screw System

Medtronic Receives FDA Clearance for Surgical Spine Device


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