Last synced on 14 November 2025 at 11:06 pm

CERTAIN BELLATEK PROVISIONAL ABUTMENTS

Page Type
Cleared 510(K)
510(k) Number
K130310
510(k) Type
Traditional
Applicant
BIOMET 3I
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2013
Days to Decision
134 days
Submission Type
Summary

CERTAIN BELLATEK PROVISIONAL ABUTMENTS

Page Type
Cleared 510(K)
510(k) Number
K130310
510(k) Type
Traditional
Applicant
BIOMET 3I
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2013
Days to Decision
134 days
Submission Type
Summary