The following data is part of a premarket notification filed by Flexible Stenting Solutions, Inc. with the FDA for Flexstent Biliary Self Expanding Stent System Model Flx-ddlll-bx.
| Device ID | K102519 |
| 510k Number | K102519 |
| Device Name: | FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | FLEXIBLE STENTING SOLUTIONS, INC. 23 CHRISTOPHER WAY SUITE 103 Eatontown, NJ 07724 |
| Contact | Joseph C Griffin, Iii |
| Correspondent | Joseph C Griffin, Iii FLEXIBLE STENTING SOLUTIONS, INC. 23 CHRISTOPHER WAY SUITE 103 Eatontown, NJ 07724 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-02 |
| Decision Date | 2010-11-22 |