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ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT

Page Type
Cleared 510(K)
510(k) Number
K103020
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2011
Days to Decision
114 days
Submission Type
Summary

ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT

Page Type
Cleared 510(K)
510(k) Number
K103020
510(k) Type
Traditional
Applicant
ATLANTIS COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2011
Days to Decision
114 days
Submission Type
Summary