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INTERGRO ORAL

Page Type
Cleared 510(K)
510(k) Number
K070147
510(k) Type
Traditional
Applicant
Biomet 3i
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2007
Days to Decision
118 days
Submission Type
Summary

INTERGRO ORAL

Page Type
Cleared 510(K)
510(k) Number
K070147
510(k) Type
Traditional
Applicant
Biomet 3i
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2007
Days to Decision
118 days
Submission Type
Summary