BONE ANCHOR SYSTEM III (BAS III)

BONE ANCHOR SYSTEM III (BAS III) is an FDA 510(k)-cleared medical device (K990295) manufactured by Boston Scientific Corp. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 4, 1999. Regulation: 8.