K-number	K111512
Device name	BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM
Applicant	Thompson Mis, Inc.
Product code	MAX
Device class	Class II
Decision date	Oct 26, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM

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