SAN ANTONIO--(BUSINESS WIRE)--CeloNova BioSciences, Inc. today announced U.S. Food and Drug Administration (FDA) 510(k) clearance expanding the indication for their leading Embozene® microsphere product to include the treatment of uterine fibroids. This approval will give women suffering from uterine fibroids an important treatment option performed by interventional radiologists called uterine fibroid embolization (UFE).
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