K-number	K211385
Device name	KeriFlex® MCP and PIP Finger Joint Prostheses
Applicant	Keri Medical SA
Product code	KYJ
Device class	Class II
Decision date	Jul 27, 2022
Decision	Substantially Equivalent
Regulation	888.3230

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Source

View the full FDA submission: accessdata.fda.gov

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KeriFlex® MCP and PIP Finger Joint Prostheses

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