K-number	K180626
Device name	Pedimax II - Pedicular Screw Spinal System
Applicant	Gm Dos Reis Industria E Comerico Ltda.
Product code	NKB
Device class	Class II
Decision date	Feb 1, 2019
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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Pedimax II - Pedicular Screw Spinal System

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