K-number	K142944
Device name	ArthroPlan Digital Templating Software
Applicant	Arthromeda, Inc.
Product code	LLZ
Device class	Class II
Decision date	Dec 16, 2014
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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ArthroPlan Digital Templating Software

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