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Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini Baseplate

Page Type
Cleared 510(K)
510(k) Number
K172502
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2018
Days to Decision
138 days
Submission Type
Summary

Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini Baseplate

Page Type
Cleared 510(K)
510(k) Number
K172502
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2018
Days to Decision
138 days
Submission Type
Summary