K-number	K173741
Device name	Reprocessed ArthoCare Ablation Wand
Applicant	Renovo, Inc.
Product code	NUJ
Device class	Class II
Decision date	Mar 5, 2018
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Reprocessed ArthoCare Ablation Wand

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