ATLANTIS ABUTMENT FOR ASTRA IMPLANT

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 For Astra Implant.

Pre-market Notification Details

Device IDK070833
510k NumberK070833
Device Name:ATLANTIS ABUTMENT FOR ASTRA IMPLANT
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 Received2007-03-27
Decision Date2007-06-22
Summary:summary

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