K-number	K101363
Device name	VU CPOD INTERVERTEBRAL BODU FUSION DEVICE
Applicant	Musculoskeletal Clinical Regulatory Advisers
Product code	ODP
Device class	Class II
Decision date	Dec 16, 2010
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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VU CPOD INTERVERTEBRAL BODU FUSION DEVICE

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