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ATLANTIS ABUTMENT IN ZIRCONIA FOR ASTRA TECH OSSEOSPEED PLUS IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112138
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2011
Days to Decision
128 days
Submission Type
Summary

ATLANTIS ABUTMENT IN ZIRCONIA FOR ASTRA TECH OSSEOSPEED PLUS IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112138
510(k) Type
Traditional
Applicant
ASTRA TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2011
Days to Decision
128 days
Submission Type
Summary