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G7 Dual Mobility System, Active Articulation System

Page Type
Cleared 510(K)
510(k) Number
K161190
510(k) Type
Special
Applicant
Biomet, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2016
Days to Decision
29 days
Submission Type
Summary

G7 Dual Mobility System, Active Articulation System

Page Type
Cleared 510(K)
510(k) Number
K161190
510(k) Type
Special
Applicant
Biomet, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2016
Days to Decision
29 days
Submission Type
Summary