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FDA 510(k)

ARx® Spinal System

K-Number: K220025 · 2022-03-31

ApplicantLife Spine, Inc.
Decision Date2022-03-31
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARx® Spinal System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2022-03-31 under approval number K220025. 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 ARx® Spinal System?

ARx® Spinal System is a medical device that received FDA 510(k) clearance on 2022-03-31. It is manufactured by Life Spine, Inc.. The 510(k) number is K220025.

When was ARx® Spinal System approved by the FDA?

ARx® Spinal System received FDA 510(k) clearance on 2022-03-31, under approval number K220025.

What company makes ARx® Spinal System?

ARx® Spinal System is manufactured by Life Spine, Inc..

What is the FDA product code for ARx® Spinal System?

The FDA product code for ARx® Spinal System is NKB.

Related Clinical Trials

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Related PubMed Literature

PMID: 41612341 Brain-computer interface commercialization. Journal of neuroengineering and rehabilitation (2026) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by Life Spine, Inc.

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Related Devices (Code: NKB)

K163301CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc. K162134ENNOVATE Spinal SystemAesculap Implant Systems, LLC K162912VIPER PRIME™ additions to the VIPER® SystemMedos International SARL K162160Preference Elite Pedicle Screw SystemAmedica Corporation K162232MOSS 100 Pedicle Screw SystemBiedermann Motech GmbH & Co. KG K162379CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc.

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.

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