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ATLANTIS(TM) ABUTMENT AND ATLANTIS(TM) CROWN ABUTMENT FOR KEYSTONE GENESIS IMPLANT, ATLANTIS GEMINI(TM) ABUTMENT...

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113003
510(k) Type
Traditional
Applicant
ASTRA TECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2012
Days to Decision
146 days
Submission Type
Summary

ATLANTIS(TM) ABUTMENT AND ATLANTIS(TM) CROWN ABUTMENT FOR KEYSTONE GENESIS IMPLANT, ATLANTIS GEMINI(TM) ABUTMENT...

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113003
510(k) Type
Traditional
Applicant
ASTRA TECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2012
Days to Decision
146 days
Submission Type
Summary