K-number	K240113
Device name	CORIOGRAPH Knee Pre-Op Plan
Applicant	Smith & Nephew, Inc.
Product code	PBF
Device class	Class II
Decision date	Mar 18, 2024
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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CORIOGRAPH Knee Pre-Op Plan

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