K-number	K101310
Device name	VU APOD INTERVERTEBRAL BODY FUSION DEVICE
Applicant	Theken Spine, LLC
Product code	OVD
Device class	Class II
Decision date	Sep 2, 2010
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 INTERVERTEBRAL BODY FUSION DEVICE

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