K-number	K091067
Device name	5.5 POLARIS SPINAL SYSTEM
Applicant	Biomet Spine
Product code	NKB
Device class	Class II
Decision date	Jul 14, 2009
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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5.5 POLARIS SPINAL SYSTEM

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