K-number	K183083
Device name	Shoreline Cervical Interbody RT System
Applicant	SeaSpine Orthopedics Corporation
Product code	ODP
Device class	Class II
Decision date	Feb 14, 2019
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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Shoreline Cervical Interbody RT System

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