# K073304: Cardica C-Port X-Change Anastomosis System and Handle and XA X-Change Subassemblies

- Pathway: 510(k) (Special)
- Applicant: Cardica, Inc.
- Decided: Dec 20, 2007 after 27 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: 12 generations back to K933887 (1993). 35 ancestors in all.
No later device cites it as a predicate yet.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063644: Cardica C-Port XA Distal Anastomosis System, Cardica, Inc. (2007) Summary page 1.

## Indications for use
The Cardica® Cardica® C-PORT® X-CHANGETM 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/K073304
Methodology: https://510kreport.com/methodology