K-number	K161223
Device name	TransContinental® M Spacers and InterContinental® Plate-Spacers
Applicant	Globus Medical, Inc.
Product code	OVD
Device class	Class II
Decision date	Jul 15, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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TransContinental® M Spacers and InterContinental® Plate-Spacers

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