# K173709: Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm

- Pathway: 510(k) (Special)
- Applicant: Inneuroco, Inc.
- Decided: Jan 26, 2018 after 53 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K010954 (2001). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171672: 065 Zenith, 074 Zenith, Inneuroco, Inc. (2017) Summary page 5.

## Indications for use
The Zenith Support Catheter is indicated for the introduction of interventional devices into the peripheral and neuro vasculature.

Source page: https://510kreport.com/device/K173709
Methodology: https://510kreport.com/methodology