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IPS E.MAX PRESS - ABUTMENT SOLUTIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120053
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2012
Days to Decision
286 days
Submission Type
Statement

IPS E.MAX PRESS - ABUTMENT SOLUTIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120053
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2012
Days to Decision
286 days
Submission Type
Statement