LORENZ PECTUS SUPPORT BAR

LORENZ PECTUS SUPPORT BAR is an FDA 510(k)-cleared medical device (K972420) manufactured by Walter Lorenz Surgical, 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 August 10, 1997. Regulation: 8.