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 |