K-number	K150600
Device name	Response 5.5/6.0 Spine System
Applicant	OrthoPediatrics Corp.
Product code	NKB
Device class	Class II
Decision date	May 22, 2015
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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Response 5.5/6.0 Spine System

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