ARTIA Reconstructive Tissue Matrix Perforated

ARTIA Reconstructive Tissue Matrix Perforated is an FDA 510(k)-cleared medical device (K162752) manufactured by Lifecell Corporation. 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 February 23, 2017. Regulation: 8.