FDA 510(k) Applications Submitted by Golden Stapler Surgical Co., Ltd.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K162707	09/28/2016	Single Use Circular Stapler, Single Use Hemorrhoidal Circular Stapler, Single Patient Use Linear Stapler and Reload, Single Patient Use Linear Cutter and Reload, Single Patient Use Endo Cutter and Reload, Single Patient Use Transverse Cutter and Reload	Golden Stapler Surgical Co., Ltd.