K221003 is an FDA 510(k) clearance for the Autosuture EEA Stapler / circular stapler with DST Series Technology / EEA Autosuture Circular Stapler with DST Series Technology / DST Series EEA Stapler / DST EEA, a Staple, Implantable (Class II — Special Controls, product code GDW), submitted by Covidien (North Haven, US). The FDA issued a Cleared decision on September 30, 2022, 178 days after receiving the submission on April 5, 2022. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4750.