K-number	K240278
Device name	Full Wedge Lateralized and Augmented Baseplates
Applicant	Fx Shoulder USA, Inc.
Product code	PHX
Device class	Class II
Decision date	May 15, 2024
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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Full Wedge Lateralized and Augmented Baseplates

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