K-number	K200792
Device name	MySpine S2-Alar/Alar-Iliac Pedicle Screw Placement Guides
Applicant	Medacta Inernational SA
Product code	PQC
Device class	Class II
Decision date	Oct 5, 2020
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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MySpine S2-Alar/Alar-Iliac Pedicle Screw Placement Guides

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