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 |