# K142265: ONE Snare Endovascular Microsnare System

- Pathway: 510(k) (Traditional)
- Applicant: Merit Medical Systems, Inc.
- Decided: Nov 13, 2014 after 90 days
- Product code: MMX (Device, Percutaneous Retrieval)
- Device class: 2
- Regulation: 21 CFR 870.5150
- 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 K914067 (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)
- K970668: The Amplantz Goose Neck Microsnare, Microvena Corp. (1998) Summary page 4.

## Indications for use
The ONE Snare Endovascular Microsnare System is intended for use in adult and pediatric populations for the retrieval and manipulation of atraumatic foreign bodies located in the coronary and peripheral cardiovascular system and the extra-cranial anatomy.

Source page: https://510kreport.com/device/K142265
Methodology: https://510kreport.com/methodology