The following data is part of a premarket notification filed by Biomet 3i with the FDA for Certain Bellatek Express And Bellatek Flex Abutments.
| Device ID | K183138 |
| 510k Number | K183138 |
| Device Name: | Certain BellaTek Express And BellaTek Flex Abutments |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | Biomet 3i 4555 Riverside Drive, Palm Beach Gardens, FL 33410 |
| Contact | Krupal Patel |
| Correspondent | Krupal Patel Biomet 3i 4555 Riverside Drive, Palm Beach Gardens, FL 33410 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-11-13 |
| Decision Date | 2019-07-02 |