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May 25, 2015 4:51 AM ET

Healthcare Equipment and Supplies

Company Overview of Spinal Elements, Inc.

Company Overview

Spinal Elements, Inc. manufactures surgical, motion preservation, and spinal fusion systems. The company offers stand-alone anterior lumbar interbody fusion devices; posterior, anterior, and cervical lumber cage systems; anterior cervical plate systems; spinal implant systems; pedicle screw systems; and facet implant systems. It has a strategic alliance with Paradigm BioDevices. The company was formerly known as Quantum Orthopedics, Inc. and changed its name in 2006. Spinal Elements, Inc. was founded in 2003 and is based in Carlsbad, California.

3115 Melrose Drive

Suite 200

Carlsbad, CA 92010

United States

Founded in 2003





Key Executives for Spinal Elements, Inc.

Chief Executive Officer and President
Vice President of Sales
Compensation as of Fiscal Year 2014.

Spinal Elements, Inc. Key Developments

Spinal Elements Announces Licensing of Essential Lateral Spinal Access and Implant Patents and 510 Product Clearance

Spinal Elements announced that they have licensed a portfolio of patents essential for accessing the lumbar spine from a lateral approach and placing implants from that approach. The lateral approach to the spine provides the potential for less disruptive, minimally invasive surgical (MIS) access techniques to address a variety of spinal pathologies. Minimally invasive spine surgery is a growing trend as more patients and surgeons seek ways to perform spinal fusions and other procedures that are less disruptive to the patients' anatomy and lives, enabling less time in the hospital for recovery and a more expedient return to daily function. The lateral spinal access procedure is a skill set that a growing number of surgeons are employing in their practices as they become trained on and comfortable with the techniques and expected outcomes for this procedure. Spinal Elements plans to use this newly licensed technology to develop access systems and implants for introduction later in the year. The company recently received 510(k) clearance from the US Food and Drug Administration (FDA) to market implants placed using the lateral access procedure. The clearance included the use of the company's Ti-Bond(R) porous titanium coating on such laterally-placed implants.

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