K-number	K160907
Device name	DePuy Actis DuoFix Hip Prosthesis
Applicant	Depuy(Ireland)
Product code	MEH
Device class	Class II
Decision date	Jul 19, 2016
Decision	Substantially Equivalent
Regulation	888.3353

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Source

View the full FDA submission: accessdata.fda.gov

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DePuy Actis DuoFix Hip Prosthesis

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