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ATLANTIS ABUTMENT FOR CAMLOG IMPLANT, DUPLICATE ABUTMENT, LATER ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110640
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2011
Days to Decision
98 days
Submission Type
Summary

ATLANTIS ABUTMENT FOR CAMLOG IMPLANT, DUPLICATE ABUTMENT, LATER ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110640
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2011
Days to Decision
98 days
Submission Type
Summary