K-number	K172467
Device name	OMNI ARC Anteverted Neck Hip Stem
Applicant	Omnilife Science
Product code	LZO
Device class	Class II
Decision date	Dec 21, 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 ARC Anteverted Neck Hip Stem

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