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ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI ABUTMENT IN ZIRCONIA FOR ASTRA IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072483
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2007
Days to Decision
73 days
Submission Type
Summary

ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI ABUTMENT IN ZIRCONIA FOR ASTRA IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072483
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2007
Days to Decision
73 days
Submission Type
Summary