MMXClass II
Device, Percutaneous Retrieval
21 CFR 870.5150 / Cardiovascular
MMX is the FDA product code for Device, Percutaneous Retrieval, a class II device type, regulated under 21 CFR 870.5150. As of , FDA records hold 32 510(k) clearances under this code, the most recent dated , and one recall.
Classification record
- Product code
- MMX
- Device name
- Device, Percutaneous Retrieval
- Regulation
- 21 CFR 870.5150
- Device class
- Class II
- Review panel
- Cardiovascular
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 32
- Ingested recalls
- 1
Clearances, product code MMX
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 2002 | 3 |
| 2003 | 2 |
| 2005 | 1 |
| 2007 | 1 |
| 2009 | 2 |
| 2010 | 1 |
| 2011 | 1 |
| 2012 | 1 |
| 2014 | 2 |
| 2015 | 2 |
| 2016 | 2 |
| 2017 | 2 |
| 2018 | 1 |
| 2019 | 1 |
| 2020 | 2 |
| 2021 | 1 |
| 2022 | 3 |
| 2023 | 2 |
| 2024 | 1 |
| 2025 | 1 |
Applicants with the most clearances
Product code MMX| Applicant | Clearances |
|---|---|
| Merit Medical Systems, Inc. | 5 |
| Argon Medical Devices, Inc | 4 |
| Cook Incorporated | 3 |
| Radius Medical Technologies, Inc. | 3 |
| Idev Technologies, Inc. | 2 |
| LimFlow Inc. | 2 |
| Abbott Medical | 1 |
| Avantec Vascular Corp. | 1 |
| Boston Scientific Corporation | 1 |
| C.R. Bard Inc | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.