The following data is part of a premarket notification filed by Biomet 3i with the FDA for 3i T3(r) External Hex Dental Implants.
| Device ID | K133049 |
| 510k Number | K133049 |
| Device Name: | 3I T3(R) EXTERNAL HEX DENTAL IMPLANTS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | BIOMET 3I 4555 RIVERSIDE DRIVE Palm Beach Gardens, FL 33410 |
| Contact | Chris Mckee |
| Correspondent | Chris Mckee BIOMET 3I 4555 RIVERSIDE DRIVE Palm Beach Gardens, FL 33410 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-09-27 |
| Decision Date | 2014-01-08 |
| Summary: | summary |