K-number	K172979
Device name	NuVasive® Growth Rod Conversion Set
Applicant	Nu Vasive, Incorporated
Product code	PGM
Device class	Class II
Decision date	Nov 6, 2017
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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NuVasive® Growth Rod Conversion Set

Everything you need for a 510(k) submission. Nothing you don't.