# MMX: Device, Percutaneous Retrieval

- Device class: 2; regulation: 21 CFR 870.5150; FDA's rule: 510(k) required
- FDA decisions: 32
- 510(k) review time 2021–2025: median 153 days (middle half 27–251)
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2016: 2
- 2017: 2
- 2018: 1
- 2019: 1
- 2020: 2
- 2021: 1
- 2022: 3
- 2023: 2
- 2024: 1
- 2025: 1

## Most-cited predicates
- K092343: EN Snare Endovascular Snare System (2009), cited by 4
- K112185: Foursnare Vascular Retrieval Snare (2011), cited by 4
- K122088: Merit One Snare System (2012), cited by 2
- K014109: IN-Time Retrieval Device (2002), cited by 2
- K021606: EN-Snare Endovascular Snare and Catheter (2002), cited by 2
- K021441: Radius Snare (2002), cited by 2
- K071457: Modification to Radius Snare (2007), cited by 2
- K170987: Captus Vascular Retrieval System (2017), cited by 1
- K181757: Günther Tulip® Vena Cava Filter Retrieval Set (2018), cited by 1
- K133681: Crux Snare Filter Retrieval Set (2014), cited by 1

Source page: https://510kreport.com/product-code/MMX
Data by year (CSV): https://510kreport.com/product-code/MMX.csv