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MULTILINK IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K090704
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2009
Days to Decision
92 days
Submission Type
Statement

MULTILINK IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K090704
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2009
Days to Decision
92 days
Submission Type
Statement