K-number	K130146
Device name	SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM
Applicant	Synthes (Usa), LLC
Product code	NDN
Device class	Class II
Decision date	May 20, 2013
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM

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