K-number	K211076
Device name	Patient Specific Marking Guides
Applicant	Additive Orthopaedics, LLC
Product code	PBF
Device class	Class II
Decision date	Jun 28, 2022
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Patient Specific Marking Guides

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