# K072525: Zipknot, Model 1017-3000

- Pathway: 510(k) (Special)
- Applicant: Medicinelodge, Inc.
- Decided: Oct 5, 2007 after 28 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The MedicineLodge ZipKnotTM is indicated for use in approximation and/or ligation of soft tissues using USP #2 braided polyethylene surgical suture.

Source page: https://510kreport.com/device/K072525
Methodology: https://510kreport.com/methodology