The following data is part of a premarket notification filed by Atlantis Components, Inc. with the FDA for Atlantis Abutment For 3i Micromini Implant.
Device ID | K062069 |
510k Number | K062069 |
Device Name: | ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | ATLANTIS COMPONENTS, INC. 8944 TAMAROA TERRACE Skokie, IL 60076 |
Contact | Betsy A Brown |
Correspondent | Betsy A Brown ATLANTIS COMPONENTS, INC. 8944 TAMAROA TERRACE Skokie, IL 60076 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-07-21 |
Decision Date | 2007-02-14 |
Summary: | summary |