K-number	K171046
Device name	SeaSpine Cambria System
Applicant	SeaSpine Orthopedics Corporation
Product code	ODP
Device class	Class II
Decision date	Jul 7, 2017
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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SeaSpine Cambria System

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