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Friday, June 20, 2008

FDA E-News Recognizes Axiom Case Study - The FDA news item was headlined, “Axiom Case Study Yields Favorable Findings with Back Pain Device.”

June 5, 2008 — A case study concerning the Axiom Worldwide’s DRX9000, published in the 2008 issue of the European Musculoskeletal Review, was mentioned in an online newsletter from the Food and Drug Administration (FDA).

The FDA news item was headlined, “Axiom Case Study Yields Favorable Findings with Back Pain Device.”

It read, in part, “A study evaluating Axiom Worldwide’s DRX9000 true

nonsurgical spinal decompression system has produced positive results. … The study chronicled a patient who underwent 22 treatments with the device over a seven-week period and reported significant pain relief at the end of the study.”

The study can be downloaded at axiomworldwide.com/research

For more information or to receive a free report on the DRX9000 call 860-633-8756.
Visit us online at CT Spine And Disc Center.
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