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While there are a variety of devices in various stages of FDA approval, there are investigational devices gaining full FDA-approval on a regular basis. The staff at RMSAS will educate you as to the current standing of all devices and help you select the right procedure for your condition.
RMSAS is now enrolling candidates for a variety DDD and spinal stenosis research trials to study alternatives to spine fusion (lumbar and cervical). These trials are a part of a U.S. Food & Drug Administration (FDA) application to gain approval for a variety of devices and procedures that have been performed in Europe for over a decade.
The clinical trials are designed to prove the safety and efficacy of these devices for treating degenerative disc disease (DDD) and other conditions typically requiring a spinal fusion. Each trial has it's own requirements. Please contact RMSAS for details.For more information on the following trials, please select your ailment below:
Spinal Stenosis - Paradigm Spine's Coflex Device
Lumbar Spinal Stenosis - Facet Solutions' Anatomic Facet Replacement System (AFRS™)
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Artificial disc replacement surgery is covered by some insurance. Please contact us to determine if you qualify. For those wanting to skip the insurance process, we do offer a global cash price as well.
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