K-number	K133363
Device name	INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
Applicant	Ldr Spine USA, Inc.
Product code	PEK
Device class	Class II
Decision date	Mar 7, 2014
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM

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