# K150936: SureClip

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Oct 23, 2015 after 199 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 K830503 (1983). 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)
- K110699: Ligamax 5, Ethicon Endo-Sugery, LLC (2011) Summary page 4.

## Indications for use
The SureClip Clip Applier is intended for use on tubular structures or vessels wherever a metal ligating clip is indicated.

Source page: https://510kreport.com/device/K150936
Methodology: https://510kreport.com/methodology