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Republic Spine Restore Cervical Interbody Fusion System

Republic Spine, LLC · Class II · Cleared Jun 19, 2019

K-numberK190889
Device nameRepublic Spine Restore Cervical Interbody Fusion System
ApplicantRepublic Spine, LLC
Product codeODP
Device classClass II
Decision dateJun 19, 2019
DecisionSubstantially Equivalent
Regulation888.3080
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Source

View the full FDA submission: accessdata.fda.gov

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