K-number	K133091
Device name	ZIP MIS INTERSPINOUS FUSION SYSTEM
Applicant	Aurora Spine
Product code	PEK
Device class	Class II
Decision date	Nov 27, 2013
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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ZIP MIS INTERSPINOUS FUSION SYSTEM

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