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Comprehensive® Convertible Glenoid - Vivacit-E Liner

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211729
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/2021
Days to Decision
153 days
Submission Type
Summary

Comprehensive® Convertible Glenoid - Vivacit-E Liner

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211729
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/2021
Days to Decision
153 days
Submission Type
Summary