K-number	K242009
Device name	360CAS Knee
Applicant	Kico Knee Innovation Company Pty, Ltd.
Product code	OLO
Device class	Class II
Decision date	Aug 8, 2024
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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360CAS Knee

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