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Glenoid Baseplate with Screw

Page Type
Cleared 510(K)
510(k) Number
K192799
510(k) Type
Traditional
Applicant
FX Shoulder USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2020
Days to Decision
144 days
Submission Type
Summary

Glenoid Baseplate with Screw

Page Type
Cleared 510(K)
510(k) Number
K192799
510(k) Type
Traditional
Applicant
FX Shoulder USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2020
Days to Decision
144 days
Submission Type
Summary