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Comprehensive Reverse Shoulder System

Page Type
Cleared 510(K)
510(k) Number
K181611
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2018
Days to Decision
97 days
Submission Type
Summary

Comprehensive Reverse Shoulder System

Page Type
Cleared 510(K)
510(k) Number
K181611
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2018
Days to Decision
97 days
Submission Type
Summary