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ATLANTIS ISUS Implant Suprastructures

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160207
510(k) Type
Traditional
Applicant
DENTSPLY INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2016
Days to Decision
237 days
Submission Type
Summary

ATLANTIS ISUS Implant Suprastructures

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160207
510(k) Type
Traditional
Applicant
DENTSPLY INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2016
Days to Decision
237 days
Submission Type
Summary