K-number	K173521
Device name	SeaSpine Cabo ACP (Anterior Cervical Plate) System
Applicant	SeaSpine Orthopedics Corporation
Product code	KWQ
Device class	Class II
Decision date	Jan 24, 2018
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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SeaSpine Cabo ACP (Anterior Cervical Plate) System

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