K-number	K161032
Device name	neon3 universal OCT spinal stabilization
Applicant	Ulrich GmbH & Co. KG
Product code	NKG
Device class	Class II
Decision date	Dec 22, 2016
Decision	Substantially Equivalent
Regulation	888.3075

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Source

View the full FDA submission: accessdata.fda.gov

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neon3 universal OCT spinal stabilization

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neon3 universal OCT spinal stabilization