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ANKYLOS

Page Type
Cleared 510(K)
510(k) Number
K012681
510(k) Type
Traditional
Applicant
DENTSPLY CERAMCO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
738 days
Submission Type
Summary

ANKYLOS

Page Type
Cleared 510(K)
510(k) Number
K012681
510(k) Type
Traditional
Applicant
DENTSPLY CERAMCO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2003
Days to Decision
738 days
Submission Type
Summary