If another company tells you that they are the owners of a 510 k that permits them to sell any of Axiom’s products, ask them for a copy of a 510K in their company name or, contact the US FDA and ask them directly.
We created the DRX9000™ True Non-Surgical Spinal Decompression™ System to assist healthcare providers in their effort to treat low (lumbar) back pain. The DRX9000™ provides a primary treatment modality for the management of pain and disability for patients suffering with incapacitating low back pain and sciatica. The system is designed to apply spinal decompressive forces to compressive and degenerative injuries of the spine. It has been found to provide reflief of pain and symptoms associated with herniated discs, bulging or protruding intervertebral discs, degenerative disc disease, posterior facet syndrome, and sciatica.
“The Axiom Worldwide website is being maintained solely for the purposes of supporting the international community. New machines are no longer available for sale in the United States and Canada. For more information, contact us.” James Gibson Jr. — President and CEO, Axiom Worldwide
NOTICE: Any company that represents that they are the “New Manufactures of Axiom Products” is providing a false and misleading representation that puts your practice, your license, and the unsuspecting patient at risk.