Reprocessed LigaSure Maryland Jaw Sealer/Divider

Reprocessed LigaSure Maryland Jaw Sealer/Divider is an FDA 510(k)-cleared medical device (K180499) manufactured by Stryker Sustainability Solutions. 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 April 22, 2018. Regulation: 8.