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ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120338
510(k) Type
Traditional
Applicant
ASTRA TECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2012
Days to Decision
153 days
Submission Type
Summary

ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120338
510(k) Type
Traditional
Applicant
ASTRA TECH INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2012
Days to Decision
153 days
Submission Type
Summary