Modification to Corlink Automated Anastomotic Device

by Bypass, Ltd. 510(k)

Active United States

510(k) K020470

Regulatory status

as of 27 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK020470	Date8 Mar 2002Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K020470
FDA Product Code: FZP
FDA applicant: Bypass , Ltd.

Device Class: Class II
Regulation: 21 CFR Part 878.4300
Advisory Committee: General, Plastic Surgery
FDA Decision: SESE Substantially Equivalent

Other devices from Bypass, Ltd.

Corlink Aad (3.5 to 6.0 M M Outer Diameter Vessels), Model 200-064, Corlink Aad (2.0 to 4.0 Mm Outer Diameter Vessels), M

Class II