# K873606: Modified Cope Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Cook, Inc.
- Decided: Jun 17, 1988 after 283 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.
7 later devices descend from it; 2 cite it directly.
0 of 8 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
- K090133: Connex Gastrointestinal Suture Anchor, Model Gias (2009), 3 descendants of its own
- K182832: Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set (2019), 2 descendants of its own
- K131201: Entuit Secure Gastrointestional Suture Anchor Set, Entuit Secure Adjustable Gastrointestinal Suture Anchor Set (2013), 2 descendants of its own
- K193612: AMT Suture Delivery System (2020), 1 descendant of its own
- K152524: Entuit Secure Gastrointestinal Suture Anchor Set, Entuit Secure Adjustable Gastrointestinal Suture Anchor Set (2015), 1 descendant of its own

Source page: https://510kreport.com/device/K873606
Methodology: https://510kreport.com/methodology