ARx Spinal System
K-Number: K200070 · 2020-04-23
Device Summary
Frequently Asked Questions
What is the ARx Spinal System?
ARx Spinal System is a medical device that received FDA 510(k) clearance on 2020-04-23. The listed applicant is Life Spine, Inc.. The 510(k) number is K200070.
When did ARx Spinal System receive FDA 510(k) clearance?
ARx Spinal System received FDA 510(k) clearance on 2020-04-23, under 510(k) number K200070.
Who is the listed applicant for ARx Spinal System?
The FDA 510(k) record lists Life Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARx Spinal System?
The FDA product code for ARx Spinal System is NKB.
Other records listing Life Spine, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NKB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.