# K133681: Crux Snare Filter Retrieval Set

- Pathway: 510(k) (Traditional)
- Applicant: Volcano Corporation
- Decided: Jan 30, 2014 after 59 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: 6 generations back to K901502 (1990). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 15 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073374: Cook Clect Vena Cava Filter, Gunther Tulip Vena Cava Filter Retrieval Set, William Cook Europe Aps (2008) Summary page 1.

## Most influential descendants
- K213494: Aveir Retrieval Catheter (2022), 0 descendants of its own

## Indications for use
The Crux" Snare Filter Retrieval Set isan endovascular medical device indicated for the retrieval of the Crux8 Vena Cava Filter (VCF) percutaneously via the jugular vein or femoral vein approach.

Source page: https://510kreport.com/device/K133681
Methodology: https://510kreport.com/methodology