K-number	K192428
Device name	AFX Femoral Implant with Inserter
Applicant	Cayenne Medical
Product code	MBI
Device class	Class II
Decision date	Oct 5, 2019
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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AFX Femoral Implant with Inserter

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