K-number	K153783
Device name	SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF
Applicant	Spinevision S.A.
Product code	MAX
Device class	Class II
Decision date	May 4, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF

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