K-number	K111913
Device name	CAPSURE(R) PS SYSTEM
Applicant	Spine Wave, Inc.
Product code	MNI
Device class	Class II
Decision date	Aug 31, 2011
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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CAPSURE(R) PS SYSTEM

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