K-number	K090132
Device name	MAXMORESPINE SPINAL SYSTEM
Applicant	Hoogland Spine Products, GmbH
Product code	HRX
Device class	Class II
Decision date	Jun 9, 2009
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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MAXMORESPINE SPINAL SYSTEM

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