K-number	K220733
Device name	OptiVu ROSA MxR
Applicant	Orthosoft Inc (D/B/A Zimmer Cas)
Product code	SBF
Device class	Class II
Decision date	Jul 29, 2022
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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OptiVu ROSA MxR

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