K-number	K063606
Device name	MODIFICATION TO STAXX FX SYSTEM
Applicant	Spine Wave, Inc.
Product code	OBL
Device class	Class II
Decision date	Apr 13, 2007
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO STAXX FX SYSTEM

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