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G7 Dual Mobility System, Active Articulation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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