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Certain BellaTek Express and BellaTek Flex Abutments

Page Type
Cleared 510(K)
510(k) Number
K183138
510(k) Type
Traditional
Applicant
Biomet 3i
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2019
Days to Decision
231 days
Submission Type
Summary

Certain BellaTek Express and BellaTek Flex Abutments

Page Type
Cleared 510(K)
510(k) Number
K183138
510(k) Type
Traditional
Applicant
Biomet 3i
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2019
Days to Decision
231 days
Submission Type
Summary