NuVasive X-CORE Mini Cervical Expandable VBR System— 510(k) K151651

Name: FDA 510(k) clearance K151651
Creator: U.S. Food and Drug Administration
Published: 2015-09-25

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K151651 for NuVasive X-CORE Mini Cervical Expandable VBR System, Substantially Equivalent on 2015-09-25. Applicant: Nu Vasive, Incorporated. Device class: 2.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code PLR
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2015-06-18
Decision date: 2015-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, 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.