K-number	K231483
Device name	MySpine Unilateral Guides
Applicant	Medacta International S.A.
Product code	PQC
Device class	Class II
Decision date	Jul 21, 2023
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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MySpine Unilateral Guides

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