K-number	K231704
Device name	Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System
Applicant	Life Spine, Inc.
Product code	OVE
Device class	Class II
Decision date	Oct 19, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System

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