NuVasive® Camber Laminoplasty System— 510(k) K191169

Name: FDA 510(k) clearance K191169
Creator: U.S. Food and Drug Administration
Published: 2019-07-03

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K191169 for NuVasive® Camber Laminoplasty System, Substantially Equivalent on 2019-07-03. Applicant: Nu Vasive, Incorporated. Device class: 2.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code NQW
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2019-05-01
Decision date: 2019-07-03
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.