K-number	K172032
Device name	Modulift Vertebral Body Replacement (VBR) System
Applicant	Aesculap Implants Systems, Inc.
Product code	PLR
Device class	Class II
Decision date	Nov 20, 2017
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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Modulift Vertebral Body Replacement (VBR) System

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