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ATLANTIS, ATLANTIS GEMINI, ATLANTIS GEMINI+ ABUTMENTS FOR ASTRA OSSEOSPEED 3.0 IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081666
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2008
Days to Decision
116 days
Submission Type
Summary

ATLANTIS, ATLANTIS GEMINI, ATLANTIS GEMINI+ ABUTMENTS FOR ASTRA OSSEOSPEED 3.0 IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081666
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2008
Days to Decision
116 days
Submission Type
Summary