NANOTITE DENTAL IMPLANTS

Implant, Endosseous, Root-form

IMPLANT INNOVATIONS, INC.

The following data is part of a premarket notification filed by Implant Innovations, Inc. with the FDA for Nanotite Dental Implants.

Pre-market Notification Details

Device IDK062432
510k NumberK062432
Device Name:NANOTITE DENTAL IMPLANTS
ClassificationImplant, Endosseous, Root-form
Applicant IMPLANT INNOVATIONS, INC. 4555 RIVERSIDE DR. Palm Beach Gardens,  FL  33410
ContactJacquelyn A Hughes
CorrespondentJacquelyn A Hughes
IMPLANT INNOVATIONS, INC. 4555 RIVERSIDE DR. Palm Beach Gardens,  FL  33410
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-08-21
Decision Date2007-02-22
Summary:summary

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.