K-number	K102636
Device name	ZENITH PEDICLE SYSTEM
Applicant	Apollo Spine, Inc.
Product code	MNH
Device class	Class II
Decision date	Mar 3, 2011
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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ZENITH PEDICLE SYSTEM

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