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Interventional Spine, Inc. Announces FDA Clearance of its Opticage™ Expandable Interbody for Treatment of Degenerative Disc Disease
Date:1/26/2012

IRVINE, Calif., Jan. 26, 2012 /PRNewswire/ -- Interventional Spine, Inc. today announced the FDA clearance of its Opticage™ Expandable Intervertebral Body Fusion Device.

(Logo: http://photos.prnewswire.com/prnh/20100419/LA88318LOGO

With the Optiport™ Access Instrument, which provides unparalleled percutaneous access to the disc space, the Opticage™ Expandable Interbody forms an integral part of Interventional Spine's revolutionary PerX360 System™. This is the first and only system in the world capable of providing surgeons the ability to perform a complete percutaneous lumbar interbody fusion via two 15mm incisions for the treatment of lumbar discogenic pain.

To date, the PerX360 System™ has been used internationally on over 20 patients, under local anesthesia, with excellent results.

Dr. David L. Greenwald, Flagler Brain and Spine Institute in St. Augustine, Florida, commented: "This is a significant milestone in the progression of making lumbar spinal fusion surgeries less invasive to patients. No other company has the cadre of technologies that allow surgeons to perform a full lumbar fusion via two 15mm incisions. To my knowledge, no other interbody fusion cage in the market has the expansion capabilities of the Opticage™. Because of this characteristic, the channel for insertion is reduced and will help minimize tissue trauma and decrease the patient overall recovery times. This is the future of spinal surgery," concluded Dr. Greenwald.

Mr. Walter A. Cuevas, Chief Executive Officer of Interventional Spine said: "This is a major milestone for the company and gives recognition to the countless hours our team, working together with Dr. Rudolf Morgenstern in Barcelona, spent in perfecting this innovative technology. We now look forward to partnering with surgeons in the United States to make this technology availabl
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SOURCE Interventional Spine, Inc.
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