# K040832: C-Port Anastomosis System (Deployment System, Clip, Accessories), Model FG-000050

- Pathway: 510(k) (Traditional)
- Applicant: Cardica, Inc.
- Decided: Nov 10, 2005 after 589 days
- Product code: FZP (Clip, Implantable)
- 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: 9 generations back to K933887 (1993). 32 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962043: Auto Suture Modified VCS Clip Applier, United States Surgical, A Division of Tyco Healthc (1996) Summary page 1.
- K020779: Proximate and Endopath Linear Cutters and Staplers, Ethicon Endo-Surgery, Inc. (2002) Summary page 1.
- K031623: Modification to Coalescent Surgical U-Clip and Accessories, Coalescent Surgical (2003) Summary page 1.
- K994160: Coalescent Surgical Sutured-Clip, Coalescent Surgical (2000) Summary page 1.

## Most influential descendants
- K053524: C-Port Distal Anastomosis System (2006), 6 descendants of its own
- K063644: Cardica C-Port XA Distal Anastomosis System (2007), 5 descendants of its own
- K090872: Modification to Cardica C-Port XA Distal Anastomosis System (2009), 1 descendant of its own
- K070548: C-Port Flexa Distal Anastomosis System (2007), 1 descendant of its own
- K101018: Cardica C-Port XA Plus Distal Anastomosis System, Model FG-000100 (2010), 0 descendants of its own

## Indications for use
The Cardica® C-PortTM Anastomosis System is intended for the creation of anastomoses in blood vessels and grafts, including use in coronary artery bypass grafting procedures.

Source page: https://510kreport.com/device/K040832
Methodology: https://510kreport.com/methodology