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COMPREHENSIVE CONVERTIBLE GLENOID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130390
510(k) Type
Traditional
Applicant
Biomet Manufacturing, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2013
Days to Decision
236 days
Submission Type
Summary

COMPREHENSIVE CONVERTIBLE GLENOID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130390
510(k) Type
Traditional
Applicant
Biomet Manufacturing, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2013
Days to Decision
236 days
Submission Type
Summary