Cleared Traditional

CD Horizon Spinal System

K223494 · Medtronic · Orthopedic

Jan 2023

Decision

63d

Days

Class 2

Risk

About This 510(k) Submission

K223494 is an FDA 510(k) clearance for the CD Horizon Spinal System, a Thoracolumbosacral Pedicle Screw System (Class II — Special Controls, product code NKB), submitted by Medtronic (Memphis, US). The FDA issued a Cleared decision on January 23, 2023, 63 days after receiving the submission on November 21, 2022. This device falls under the Orthopedic review panel. Regulated under 21 CFR 888.3070.

Submission Details

510(k) Number	K223494 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 21, 2022
Decision Date	January 23, 2023
Days to Decision	63 days
Submission Type	Traditional
Review Panel	Orthopedic (OR)
Summary	Summary PDF

Device Classification

Product Code	NKB — Thoracolumbosacral Pedicle Screw System
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 888.3070
Definition	Intended To Provide Immobilization And Stabilization Of Spinal Segments In Thoracic, Lumbar, And Sacral Spine As An Adjunct To Fusion.