# K900923: Zimmon Endoscopic Pancreatic Stent

- Pathway: 510(k) (Traditional)
- Applicant: Wilson-Cook Medical, Inc.
- Decided: Oct 26, 1990 after 241 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
No predicates in its family tree.
10 later devices descend from it; 4 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K133700: Advanix Pancreatic Stent and Naviflex Rapid Exchange Pancreatic Delivery System and Pushers (2014), 4 descendants of its own
- K172057: Zimmon Pancreatic Stents/Stent sets, Geenen Pancreatic Stents/Stent Sets, Pushing Catheter and Guiding Catheter, Johlin Pancreatic Wedge Stent and Introducer Set (2018), 2 descendants of its own
- K243412: ARCHIMEDES Biodegradable Pancreatic Stent (2025), 1 descendant of its own
- K223592: Advanix™ Pancreatic Stent and NaviFlex™ Rapid Exchange (RX) Pancreatic Delivery System and Pushers (2022), 1 descendant of its own
- K260835: ARCHIMEDES Biodegradable Stent (Medium) (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K900923
Methodology: https://510kreport.com/methodology