K-number	K151056
Device name	Aesculap T-Space PEEK and XP Spinal System
Applicant	Aesculap Implant Systems, LLC
Product code	MAX
Device class	Class II
Decision date	Aug 13, 2015
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Aesculap T-Space PEEK and XP Spinal System

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