Healthcare Industry News:  degenerative disc disease 

Devices Orthopaedic Neurosurgery

 News Release - March 10, 2011

Medtronic Introduces VERTEX SELECT(R) CHROMALOY(TM) Plus Rods

Offering Surgeons An Additional Rod Material Option To Treat The Occipitocervical and Upper-Thoracic Spine

MEMPHIS, Tenn.--(Healthcare Sales & Marketing Network)-- Continuing its leadership in cervical spine medical device therapies, Medtronic, Inc. (NYSE:MDT ) today announced the U.S. launch of VERTEX SELECT® CHROMALOY™ Plus Rods. The announcement was made at the 27th annual meeting of the American Association of Neurological Surgeons/ Congress of Neurological Surgeons Section of Disorders of the Spine and Peripheral Nerves in Phoenix.

The VERTEX SELECT® CHROMALOY™ Plus Rod is a supplement to the VERTEX SELECT® Reconstruction System. During a procedure, a surgeon uses the rods to connect existing or new fusion systems in the patient’s occipitocervical and upper-thoracic spine. CHROMALOY™ Rods consist of cobalt chrome alloy material with engineered features, including a blend of three metals which, according to mechanical testing, help improve the rod's biomechanical characteristics and maintain a more rigid overall construct. The VERTEX SELECT® Reconstruction System is intended to provide stabilization to promote fusion.

“The addition of the CHROMALOY™ Plus Rods further differentiates the VERTEX® System by providing a surgeon a choice among multiple rod diameters and material options to better accommodate patient anatomy and pathology,” said Doug King, Senior Vice President and President of Medtronic Spinal.

The VERTEX SELECT® Reconstruction System consists of implants and general instruments that can be used to surgically treat patients with a variety of conditions that can contribute to spinal instability, including degenerative disc disease, spinal stenosis, fracture, tumors, and/or spondylolisthesis. The VERTEX® System product line has more than 10 years of clinical experience and has been used in more than 100,000 cases.

Potential risks associated with the use of the device include, but are not limited to: bending, and/or breakage of any or all of the components. A successful result may not be achieved in every case.

About the Spine Business at Medtronic

The Spine business, based in Memphis, Tenn., is the global leader in today’s spine market and is committed to advancing the treatment of spinal conditions. The Spine business collaborates with world-renowned surgeons, researchers and innovative partners to offer state-of-the-art products and technologies for neurological, orthopaedic and spinal conditions. Medtronic is committed to developing affordable, minimally invasive procedures that provide lifestyle friendly surgical therapies. More information about the company and its spinal treatments can be found at and its patient-education Web sites,,, and

About Medtronic

Medtronic, Inc. (, headquartered in Minneapolis, is the global leader in medical technology – alleviating pain, restoring health, and extending life for millions of people around the world.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic’s periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

Source: Medtronic

Issuer of this News Release is solely responsible for its content.
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