The following data is part of a premarket notification filed by Alveolus, Inc. with the FDA for Endoventions Alimaxx-e Esophageal Stent System.
| Device ID | K051621 |
| 510k Number | K051621 |
| Device Name: | ENDOVENTIONS ALIMAXX-E ESOPHAGEAL STENT SYSTEM |
| Classification | Prosthesis, Esophageal |
| Applicant | ALVEOLUS, INC. 9013 PERIMETER WOODS SUITE A Charlotte, NC 28216 |
| Contact | Donald V Canal |
| Correspondent | Donald V Canal ALVEOLUS, INC. 9013 PERIMETER WOODS SUITE A Charlotte, NC 28216 |
| Product Code | ESW |
| CFR Regulation Number | 878.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-06-20 |
| Decision Date | 2005-07-11 |
| Summary: | summary |