The following data is part of a premarket notification filed by Coltene, Inc. with the FDA for Coltene Brilliant D.i. Direct Inlay System.
| Device ID | K870266 |
| 510k Number | K870266 |
| Device Name: | COLTENE BRILLIANT D.I. DIRECT INLAY SYSTEM |
| Classification | Material, Tooth Shade, Resin |
| Applicant | COLTENE, INC. C/O ROBERT BAUER & ASSOCIATES 111 N. WABASH Chicago, IL 60602 |
| Contact | Bauer, Phd |
| Correspondent | Bauer, Phd COLTENE, INC. C/O ROBERT BAUER & ASSOCIATES 111 N. WABASH Chicago, IL 60602 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-23 |
| Decision Date | 1987-02-27 |