K-number	K173864
Device name	Peekplus® Interbody Fusion Device
Applicant	Vallum Corporation
Product code	MAX
Device class	Class II
Decision date	Jul 2, 2018
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Peekplus® Interbody Fusion Device

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