Last synced on 27 January 2023 at 11:04 pm

ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT FOR NOBEL REPLACE IMPLANTS, ATLANTIS GEMINI + ABUTMENT FOR NOBEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091920
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2009
Days to Decision
90 days
Submission Type
Summary

ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT FOR NOBEL REPLACE IMPLANTS, ATLANTIS GEMINI + ABUTMENT FOR NOBEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091920
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2009
Days to Decision
90 days
Submission Type
Summary