K251123 is an FDA 510(k) clearance for the Niti-S Biliary Stent; Niti-S Biliary Slim M Stent, a Stents, Drains And Dilators For The Biliary Ducts (Class II — Special Controls, product code FGE), submitted by Taewoong Medical Co., Ltd. (Gyeonggi-Do, KR). The FDA issued a Cleared decision on December 29, 2025, 262 days after receiving the submission on April 11, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5010.
| 510(k) Number | K251123 FDA.gov |
| FDA Decision | Cleared SESU |
| Date Received | April 11, 2025 |
| Decision Date | December 29, 2025 |
| Days to Decision | 262 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FGE — Stents, Drains And Dilators For The Biliary Ducts |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5010 |