K-number	K133340
Device name	SPINEWORKS ANTERIOR LUMBAR DEVICE
Applicant	Spineworks, LLC
Product code	MAX
Device class	Class II
Decision date	Apr 11, 2014
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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SPINEWORKS ANTERIOR LUMBAR DEVICE

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