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CERVITEC PLUS

Page Type
Cleared 510(K)
510(k) Number
K072338
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2007
Days to Decision
32 days
Submission Type
Statement

CERVITEC PLUS

Page Type
Cleared 510(K)
510(k) Number
K072338
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2007
Days to Decision
32 days
Submission Type
Statement