PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES

PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES is an FDA 510(k)-cleared medical device (K011206) manufactured by Parallax Medical, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 2001. Regulation: 8.