K182910 is an FDA 510(k) clearance for the Segmented Esophageal Stent System. This device is classified as a Prosthesis, Esophageal (Class II - Special Controls, product code ESW).
Submitted by Micro-Tech (Nanjing) Co., Ltd. (Nanjing, CN). The FDA issued a Cleared decision on May 29, 2019, 224 days after receiving the submission on October 17, 2018.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 878.3610.
| 510(k) Number | K182910 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 17, 2018 |
| Decision Date | May 29, 2019 |
| Days to Decision | 224 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | ESW — Prosthesis, Esophageal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3610 |