K-number	K081195
Device name	REVERE UNIPLANAR SCREWS
Applicant	Globus Medical, Inc.
Product code	NKB
Device class	Class II
Decision date	May 28, 2008
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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REVERE UNIPLANAR SCREWS

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