Last synced on 20 December 2024 at 11:05 pm

ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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