K-number	K163303
Device name	OsteoMed ExtremiFix Mid and Large Screw System
Applicant	Osteomed, LLC
Product code	HWC
Device class	Class II
Decision date	Apr 4, 2017
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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OsteoMed ExtremiFix Mid and Large Screw System

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