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ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062069
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2007
Days to Decision
208 days
Submission Type
Summary

ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062069
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2007
Days to Decision
208 days
Submission Type
Summary