K-number	K132191
Device name	SP-FIX SPINOUS PROCESS FIXATION PLATE
Applicant	Globus Medical, Inc.
Product code	PEK
Device class	Class II
Decision date	Nov 22, 2013
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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SP-FIX SPINOUS PROCESS FIXATION PLATE

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