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Univers Revers Modular Glenoid System (Augemented baseplates)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193372
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2020
Days to Decision
36 days
Submission Type
Summary

Univers Revers Modular Glenoid System (Augemented baseplates)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193372
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2020
Days to Decision
36 days
Submission Type
Summary