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ANKYLOS DENTAL IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K040946
510(k) Type
Traditional
Applicant
FRIADENT GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2004
Days to Decision
80 days
Submission Type
Summary

ANKYLOS DENTAL IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K040946
510(k) Type
Traditional
Applicant
FRIADENT GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2004
Days to Decision
80 days
Submission Type
Summary