SAN ANTONIO--(BUSINESS WIRE)--Vidacare, the leading developer, manufacturer and marketer of advanced intraosseous technology, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration to market its new bone marrow biopsy (trephine) system. With its lithium-powered driver, Vidacare’s OnControl™ Bone Marrow Biopsy System represents the first effort in decades to improve the speed, control, core capture rate, and patient comfort of the bone marrow biopsy procedure.
