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Lanx, Inc. Announces Aspen™ Spinous Process Fixation System Clinical Data at IMAST
Date:7/25/2011

ing flexion-extension, lateral bending and axial rotation. In the combined average range of motion, both the Aspen device with bilateral facet screws and bilateral pedicle screws provided statistically superior stability.

To date, over 800 spine surgeons have used the Aspen system in nearly 20,000 implantations to achieve lumbar fusion in a less invasive manner than pedicle screws. The system includes a proprietary spiked fixation plate designed to be rigidly affixed to the spinous processes with the use of specialized surgical instrumentation. The unique central barrel allows the device to share the weight found in the lumbar and thoracic spine, while its hollow and fenestrated design serves as a bone graft containment chamber to facilitate fusion.

The Aspen system is intended for single level use in the thoracic or lumbar spine (T1-S1) for the treatment of degenerative disc disease, spondylolisthesis, spinal trauma or spinal tumor. The Aspen system is currently being used in a wide range of surgical applications including posterior fusions and interbody fusions.

Lanx markets a full line of spine stabilization technologies. For more information about the Aspen system or Lanx, please visit www.lanx.com.

About Lanx, Inc.Lanx is one of the largest and fastest growing privately held global spine companies. The Company was founded by a team of experienced medical device professionals and engineers in 2003 to improve the quality of spine care and provide surgeons with innovative products. Lanx develops and markets a full line of fusion technologies with a focus on minimally invasive and biologics products. The Company is headquartered in Broomfield, CO. More information on Lanx and its spinal surgery products can be found at www.lanx.com.Company Contact:

Media / Investors:Steve Deitsch

Kim Muscara / Nick LaudicoChief Financial Officer

(646) 536-7011/
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