K-number	K220888
Device name	MySpine S2-SI Pedicle and Sacro-Iliac Screw Placement Guides
Applicant	Medacta International S.A.
Product code	QSR
Device class	Class II
Decision date	May 24, 2022
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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MySpine S2-SI Pedicle and Sacro-Iliac Screw Placement Guides

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