K-number	K171156
Device name	OMNI Anseris Hip Stem
Applicant	Omnilife Science
Product code	LZO
Device class	Class II
Decision date	Aug 17, 2017
Decision	Substantially Equivalent
Regulation	888.3353

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Source

View the full FDA submission: accessdata.fda.gov

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OMNI Anseris Hip Stem

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