AOS IMPLANT TUBES, IMPLANT NEEDLES & RETAINING BOTTONS

AOS IMPLANT TUBES, IMPLANT NEEDLES & RETAINING BOTTONS is an FDA 510(k)-cleared medical device (K062826) manufactured by Alpha-Omega Services, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 2007. Regulation: 8.