K-number	K081952
Device name	SYNERGY SPINAL SYSTEM (6.35 POLARIS)
Applicant	Biomet Spine
Product code	NKB
Device class	Class II
Decision date	Oct 7, 2008
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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SYNERGY SPINAL SYSTEM (6.35 POLARIS)

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