# K011589: 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

- Pathway: 510(k) (Traditional)
- Applicant: Bypass, Ltd.
- Decided: Dec 26, 2001 after 217 days
- Product code: NCA (Clip, Implantable, For Coronary Artery Bypass Graft (Cabg))
- Device class: 2
- Regulation: 21 CFR 878.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K864146 (1986). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K970793: Implantable Clip, United States Surgical, A Division of Tyco Healthc (1997) Summary page 4.
- K933887: Implantable Clip, United States Surgical, A Division of Tyco Healthc (1993) Summary page 4.
- K864146: Deknatel Gwathmey Vascular Stapling Kit (Tenative), Cardio Thoracic Systems (1986) Summary page 4.

## Most influential descendants
- K020470: Modification to Corlink Automated Anastomotic Device (2002), 1 descendant of its own
- K033979: Corlink Automated Anastomotic System (2004), 0 descendants of its own

## Indications for use
The ByPass CorLink™ Anastomotic Device is intended to create vascular anastomoses between blood vessels. Specifically, the device is indicated for creation of a sutureless proximal anastomosis between a venous graft conduit and the aorta for coronary artery bypass grafting (CABG) procedures.

Source page: https://510kreport.com/device/K011589
Methodology: https://510kreport.com/methodology