K-number	K180498
Device name	NuVasive Reline Fenestrated Screws, High V+ Bone Cement
Applicant	Nu Vasive, Incorporated
Product code	PML
Device class	Class II
Decision date	Nov 28, 2018
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive Reline Fenestrated Screws, High V+ Bone Cement

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