K-number	K082712
Device name	THEKEN SPINE VU EPOD AND VU LPOD SYSTEM
Applicant	Theken Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Jan 2, 2009
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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THEKEN SPINE VU EPOD AND VU LPOD SYSTEM

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