K-number	K201471
Device name	M-Vizion Femoral Revision System Extension
Applicant	Medacta International S.A.
Product code	LZO
Device class	Class II
Decision date	Jan 11, 2021
Decision	Substantially Equivalent
Regulation	888.3353

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Source

View the full FDA submission: accessdata.fda.gov

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M-Vizion Femoral Revision System Extension

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