MUM
- Product code
- MUM
- Device name
- Stent, Metallic, Expandable, Duodenal
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.3610
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 6
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K250663 | 2025-03-31 | Taewoong Medical Co., Ltd. | Niti-S Duodenal Comfort Stent, Niti-S Colonic Comfor |
Official FDA classification page: MUM
Classification and pathway per current FDA publications. Data from openFDA (CC0).