RABEA DEVICE, MODEL PXXXXXX

RABEA DEVICE, MODEL PXXXXXX is an FDA 510(k)-cleared medical device (K990345) manufactured by Signus Medizintechnik GmbH. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 29, 1999. Regulation: 8.