K-number	K131615
Device name	POLARIS SPINAL SYSTEM
Applicant	Biomet Spine (Aka Ebi, LLC)
Product code	OSH
Device class	Class II
Decision date	Sep 4, 2013
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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POLARIS SPINAL SYSTEM

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