The following data is part of a premarket notification filed by Bicon, Inc. with the FDA for The 5.0 X 6.0mm Dental Implant.
| Device ID | K062044 |
| 510k Number | K062044 |
| Device Name: | THE 5.0 X 6.0MM DENTAL IMPLANT |
| Classification | Implant, Endosseous, Root-form |
| Applicant | BICON, INC. 501 ARBORWAY Boston, MA 02130 |
| Contact | Vincent J Morgan |
| Correspondent | Vincent J Morgan BICON, INC. 501 ARBORWAY Boston, MA 02130 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-07-19 |
| Decision Date | 2006-11-21 |