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Saturday, 11/10/2018 2:29:51 PM

Saturday, November 10, 2018 2:29:51 PM

Post# of 333959
Dr. Koneru, who led the discussion, expressed confidence in the FDA’s constructive feedback. “We are pleased that the FDA viewed our data and statistical methods favorably. They have provided guidance on how to combine the back-pain study results, along with our previously cleared 510(k), into a single 510(k) submission for obtaining expedited expanded market clearance.”, he said.