K011817 is an FDA 510(k) clearance for the BRIDGE FX. This device is classified as a Stents, Drains And Dilators For The Biliary Ducts (Class II - Special Controls, product code FGE).
Submitted by Medtronic Ave, Inc. (Santa Rosa, US). The FDA issued a Cleared decision on August 22, 2001, 72 days after receiving the submission on June 11, 2001.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5010.
| 510(k) Number | K011817 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Abbreviated 510(k) (SESU) |
| Date Received | June 11, 2001 |
| Decision Date | August 22, 2001 |
| Days to Decision | 72 days |
| Submission Type | Special |
| 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 |