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FDA 510(k)

ARx Illiac Spinal Screw System

K-Number: K203163 · 2020-12-17

Decision Date2020-12-17
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARx Illiac Spinal Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine, Inc.. It received FDA 510(k) clearance on 2020-12-17 under 510(k) number K203163. 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 Illiac Spinal Screw System?

ARx Illiac Spinal Screw System is a medical device that received FDA 510(k) clearance on 2020-12-17. The listed applicant is Life Spine, Inc.. The 510(k) number is K203163.

When did ARx Illiac Spinal Screw System receive FDA 510(k) clearance?

ARx Illiac Spinal Screw System received FDA 510(k) clearance on 2020-12-17, under 510(k) number K203163.

Who is the listed applicant for ARx Illiac Spinal Screw 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 Illiac Spinal Screw System?

The FDA product code for ARx Illiac Spinal Screw 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.

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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

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