# K091017: Cardica Pas-Port Proximal Anastomosis System, Model FG-000001

- Pathway: 510(k) (Special)
- Applicant: Cardica, Inc.
- Decided: Apr 29, 2009 after 20 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: 3 generations back to K970793 (1997). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081225: Cardica Pas-Port Proximal Anastomosis System, Cardica, Inc. (2008) Summary page 2.

## Most influential descendants
- K202124: Aesculap PAS-Port Proximal Anastomosis System (2020), 0 descendants of its own

## Indications for use
The Cardica® PAS-Port® Proximal Anastomosis System is intended to create the aortic anastomosis of aortic autologous vein grafts.

Source page: https://510kreport.com/device/K091017
Methodology: https://510kreport.com/methodology