K-number	K141930
Device name	OSSEOFLEX SB, 10G/4ML, OSSEOFLEX SB, 10G/2ML
Applicant	Osseon, LLC
Product code	NDN
Device class	Class II
Decision date	Aug 21, 2014
Decision	Substantially Equivalent
Regulation	888.3027

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View the full FDA submission: accessdata.fda.gov

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OSSEOFLEX SB, 10G/4ML, OSSEOFLEX SB, 10G/2ML

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