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

Name: FDA 510(k) clearance K172032
Creator: U.S. Food and Drug Administration
Published: 2017-11-20

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.. Device class: 2.

Clearance details

Applicant: Aesculap Implants Systems, Inc.
Product code: Code PLR
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2017-07-05
Decision date: 2017-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.