Last synced on 14 November 2025 at 11:06 pm

Full Wedge Lateralized and Augmented Baseplates

Page Type
Cleared 510(K)
510(k) Number
K240278
510(k) Type
Traditional
Applicant
FX Shoulder USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2024
Days to Decision
104 days
Submission Type
Summary

Full Wedge Lateralized and Augmented Baseplates

Page Type
Cleared 510(K)
510(k) Number
K240278
510(k) Type
Traditional
Applicant
FX Shoulder USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2024
Days to Decision
104 days
Submission Type
Summary