The following data is part of a premarket notification filed by Endochoice, Inc. with the FDA for Bonastent Tracheal / Bronchial.
| Device ID | K140472 |
| 510k Number | K140472 |
| Device Name: | BONASTENT TRACHEAL / BRONCHIAL |
| Classification | Prosthesis, Tracheal, Expandable |
| Applicant | ENDOCHOICE, INC. 1208-12 ROCKFORD RD. Toronto, On, CA M2r 3a2 |
| Contact | Bosmat Friedman |
| Correspondent | Bosmat Friedman ENDOCHOICE, INC. 1208-12 ROCKFORD RD. Toronto, On, CA M2r 3a2 |
| Product Code | JCT |
| CFR Regulation Number | 878.3720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-02-25 |
| Decision Date | 2014-10-17 |
| Summary: | summary |