NuVasive CoRoent Thoracolumbar Implants— 510(k) K150994

Name: FDA 510(k) clearance K150994
Creator: U.S. Food and Drug Administration
Published: 2015-06-17

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K150994 for NuVasive CoRoent Thoracolumbar Implants, Substantially Equivalent on 2015-06-17. Applicant: Nu Vasive, Incorporated. Device class: 2.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code PHM
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2015-04-15
Decision date: 2015-06-17
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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