# K991674: Cordis Palmaz Corinthian Transhepatic Biliary Stent and Delivery System, Models PC155BJS, PCI156BJS, PC185BJS, PC186BJS

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Aug 12, 1999 after 87 days
- Product code: FGE (Stents, Drains And Dilators For The Biliary Ducts)
- Device class: 2
- Regulation: 21 CFR 876.5010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K905720 (1991). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990631: Cordia Palmaz Corinthian Transhepatic Biliary Stent and Delivery System, Model PC125BPS, PC126BPS, PC127BPS,PC128BPS, PC, Cordis Corp. (1999) Summary page 1.

## Indications for use
The Cordis PALMAZ CORINTHIAN Stent and Delivery System is indicated for the palliation of malignant neoplasms in the biliary tree.

Source page: https://510kreport.com/device/K991674
Methodology: https://510kreport.com/methodology