K-number	K132968
Device name	UNIVISE SPINOUS PROCESS FIXATION PLATE (35MM, 40MM)
Applicant	Stryker Spine
Product code	PEK
Device class	Class II
Decision date	Nov 18, 2013
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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UNIVISE SPINOUS PROCESS FIXATION PLATE (35MM, 40MM)

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