K-number	K191779
Device name	Attune Revision LPS Inserts
Applicant	Depuy(Ireland)
Product code	KRO
Device class	Class II
Decision date	Oct 8, 2019
Decision	Substantially Equivalent
Regulation	888.3510

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Source

View the full FDA submission: accessdata.fda.gov

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Attune Revision LPS Inserts

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