K-number	K080822
Device name	VU APOD INTERVERTABRAL BODY FUSION DEVICE
Applicant	Theken Spine, LLC
Product code	OVD
Device class	Class II
Decision date	Jul 2, 2008
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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VU APOD INTERVERTABRAL BODY FUSION DEVICE

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