C-VBR— 510(k) K152568

Substantially Equivalent

Cardinal Spine, LLC

FDA 510(k) clearance K152568 for C-VBR, Substantially Equivalent on 2016-02-11. Applicant: Cardinal Spine, LLC. Device class: 2.

Clearance details

Applicant: Cardinal Spine, LLC
Product code: Code PLR
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2015-09-09
Decision date: 2016-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, KY, US

Download summary PDF View on FDA.gov ↗

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