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Providence Medical Technology Gains FDA Clearance for DTRAX Spinal System -

Providence Medical Technology received FDA 510(k) clearance to market its DTRAX® Spinal System for use in posterior cervical fusion in patients with degenerative disc disease. This 510(k) provides a more specific indication for DTRAX, which was a Class I device with a broad indication for fusion.The DTRAX Spinal System is reportedly the only sterile-packaged, single-use set of instruments specifically cleared for posterior cervical fusion. (Providence Medical Technology, 5/22/18)