The following data is part of a premarket notification filed by Implant Innovations, Inc. with the FDA for Nanotite Dental Implants.
Device ID | K062432 |
510k Number | K062432 |
Device Name: | NANOTITE DENTAL IMPLANTS |
Classification | Implant, Endosseous, Root-form |
Applicant | IMPLANT INNOVATIONS, INC. 4555 RIVERSIDE DR. Palm Beach Gardens, FL 33410 |
Contact | Jacquelyn A Hughes |
Correspondent | Jacquelyn A Hughes IMPLANT INNOVATIONS, INC. 4555 RIVERSIDE DR. 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 | 2006-08-21 |
Decision Date | 2007-02-22 |
Summary: | summary |