Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider

Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider is an FDA 510(k)-cleared medical device (K172856) 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 November 15, 2017. Regulation: 8.