CD Horizon Spinal System
K-Number: K223494 · 2023-01-23
ApplicantMedtronic
Decision Date2023-01-23
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CD Horizon Spinal System is a medical device manufactured by Medtronic. It received FDA 510(k) clearance on 2023-01-23 under approval number K223494. The device is classified under product code NKB. It was reviewed by the OR 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 2023-01-23. It is manufactured by Medtronic. The 510(k) number is K223494.
When was CD Horizon Spinal System approved by the FDA?
CD Horizon Spinal System received FDA 510(k) clearance on 2023-01-23, under approval number K223494.
What company makes CD Horizon Spinal System?
CD Horizon Spinal System is manufactured by Medtronic.
What is the FDA product code for CD Horizon Spinal System?
The FDA product code for CD Horizon Spinal System is NKB.
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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.