ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE

Abutment, Implant, Dental, Endosseous

ATLANTIS COMPONENTS, INC.

The following data is part of a premarket notification filed by Atlantis Components, Inc. with the FDA for Atlantis Abutment In Zirconia For 3i Certain Interface.

Pre-market Notification Details

Device IDK063734
510k NumberK063734
Device Name:ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE
ClassificationAbutment, Implant, Dental, Endosseous
Applicant ATLANTIS COMPONENTS, INC. 8944 TAMAROA TERRACE Skokie,  IL  60076
ContactBetsy A Brown
CorrespondentBetsy A Brown
ATLANTIS COMPONENTS, INC. 8944 TAMAROA TERRACE Skokie,  IL  60076
Product CodeNHA  
CFR Regulation Number872.3630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-12-18
Decision Date2007-03-02
Summary:summary

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