K-number	K182949
Device name	Healix Compression Screw System
Applicant	Nvision Biomedical Technologies, LLC
Product code	HWC
Device class	Class II
Decision date	Dec 4, 2018
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Healix Compression Screw System

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Healix Compression Screw System