Nuvectra Submits Chemical Composition and Biocompatibility Data to FDA for Virtis™
NUVECTRA CORP COMMON (NVTR)
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Source: GlobeNewswire
PLANO, Texas, Oct. 18, 2019 (GLOBE NEWSWIRE) -- Nuvectra Corporation (NASDAQ: NVTR), a neurostimulation medical device company, today announced it has submitted supplementary chemical composition and biocompatibility data to the U.S. Food and Drug Administration (FDA) in support of the Company’s Virtis pre-market approval (PMA) application for the treatment of chronic urinary retention and symptoms of overactive bladder. Fred Parks, Chief Executive Officer, commented, “In April of this year, the FDA requested additional information on chemical composition and biocompatibility regarding our Virtis PMA application. Today, with all requested studies favorably concluded, we submitted the results to the FDA and believe we have fully satisfied their request for supplemental toxicity and biocompatibility data. I’d like to thank the Nuvectra team, led by Chief Technical Operations Officer Ben Tranchina, and our partners for their diligence and timely efforts of this critical milestone. We
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