Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CD Horizon™ Spinal System

K-Number: K231184 · 2023-05-26

Decision Date2023-05-26
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CD Horizon™ Spinal System is a medical device manufactured by Medtronic Sofamor Danek USA, Inc.. It received FDA 510(k) clearance on 2023-05-26 under approval number K231184. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CD Horizon™ Spinal System?

CD Horizon™ Spinal System is a medical device that received FDA 510(k) clearance on 2023-05-26. It is manufactured by Medtronic Sofamor Danek USA, Inc.. The 510(k) number is K231184.

When was CD Horizon™ Spinal System approved by the FDA?

CD Horizon™ Spinal System received FDA 510(k) clearance on 2023-05-26, under approval number K231184.

What company makes CD Horizon™ Spinal System?

CD Horizon™ Spinal System is manufactured by Medtronic Sofamor Danek USA, Inc..

What is the FDA product code for CD Horizon™ Spinal System?

The FDA product code for CD Horizon™ Spinal System is OLO.

Related Clinical Trials

Related PubMed Literature

Other Devices by Medtronic Sofamor Danek USA, Inc.

View all 76 devices →

Related Devices (Code: OLO)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.