PHOENIX BONE SCREWS PBS-TYPE SERIES

PHOENIX BONE SCREWS PBS-TYPE SERIES is an FDA 510(k)-cleared medical device (K930125) manufactured by Phoenix Bioengineering, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 29, 1993. Regulation: 8.