K-number	K151705
Device name	Lotus Posterior Cervical/Thoracic Spinal System
Applicant	Spinal Elements, Inc.
Product code	NKG
Device class	Class II
Decision date	Sep 3, 2015
Decision	Substantially Equivalent
Regulation	888.3075

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View the full FDA submission: accessdata.fda.gov

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Lotus Posterior Cervical/Thoracic Spinal System

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