Modulift Vertebral Body Replacement (VBR) System— 510(k) K172032

Substantially Equivalent

Aesculap Implants Systems, Inc.

FDA 510(k) clearance K172032 for Modulift Vertebral Body Replacement (VBR) System, Substantially Equivalent on 2017-11-20. Applicant: Aesculap Implants Systems, Inc..

Clearance details

Applicant: Aesculap Implants Systems, Inc.
Product code: Code PLR
Advisory panel: Orthopedic
Date received: 2017-07-05
Decision date: 2017-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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