Statement of Compliance with California Law

Effective July 1, 2013, to the best of our knowledge, Ortho Kinematics Inc. ("OKI") is in compliance with a Comprehensive Compliance Program (“CCP”) that satisfies the requirements of California Health and Safety Code §§ 119400-119402, based on our good faith understanding of the statutory provisions as they may apply to a medical device manufacturer.

Consistent with the Department of Health and Human Services Office of the Inspector General Compliance Program Guidance for Pharmaceutical Manufacturers ("HHS-OIG Guidance"), OKI has tailored its CCP to the nature of its business as a medical device manufacturer.1

In addition to our CCP, OKI has established an annual spending limit for certain promotional activities directed toward healthcare professionals practicing in California ("Annual Spending Limit"). The Annual Spending Limit applies to educational items, promotional materials, and other items or activities that are provided to a California healthcare professional, as defined by and required by the California Health and Safety Code §§ 119400-119402.

OKI is committed to the highest standards of ethical and legal conduct. We have developed a CCP that is reasonably designed to prevent and detect violations, and includes the following:

To obtain a print version of our CCP or this declaration, please call Customer Support at 1 (512) 334-5490, or for toll-free communications please email info@orthokinematics.com. To report potential violations of OKI's CCP, please complete a Compliance Report Form, and mail it to:

Ortho Kinematics
Compliance Officer
110 Wild Basin Road
Suite 250
Austin, TX 78746

1 While California Health and Safety Code §§ 119400-119402 makes reference to compliance with the Pharmaceutical Research and Manufacturers of America’s Code on Interactions with Healthcare Professionals (“PhRMA Code”), OKI manufactures medical devices rather than pharmaceutical products. Therefore, OKI adopted policies and procedures consistent with The AdvaMed Code of Ethics on Interactions with Healthcare Professionals (“AdvaMed Code”) which, although substantially similar to the PhRMA Code, recognizes differences applicable to the medical device industry.