K-number	K223529
Device name	PressON Spinal Fixation System
Applicant	Nexus Spine, LLC
Product code	NKB
Device class	Class II
Decision date	May 2, 2023
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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PressON Spinal Fixation System

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