Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is an FDA 510(k)-cleared medical device (K220411) 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 May 12, 2022. Regulation: 8.