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ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063734
510(k) Type
Traditional
Applicant
Atlantis Components, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2007
Days to Decision
74 days
Submission Type
Summary

ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063734
510(k) Type
Traditional
Applicant
Atlantis Components, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2007
Days to Decision
74 days
Submission Type
Summary