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FDA 510(k)

Revolution Spinal Fixation System

K-Number: K160216 · 2016-04-22

Decision Date2016-04-22
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Revolution Spinal Fixation System is a medical device manufactured by Intelligent Implant Systems, LLC. It received FDA 510(k) clearance on 2016-04-22 under approval number K160216. 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 Revolution Spinal Fixation System?

Revolution Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2016-04-22. It is manufactured by Intelligent Implant Systems, LLC. The 510(k) number is K160216.

When was Revolution Spinal Fixation System approved by the FDA?

Revolution Spinal Fixation System received FDA 510(k) clearance on 2016-04-22, under approval number K160216.

What company makes Revolution Spinal Fixation System?

Revolution Spinal Fixation System is manufactured by Intelligent Implant Systems, LLC.

What is the FDA product code for Revolution Spinal Fixation System?

The FDA product code for Revolution Spinal Fixation System is NKB.

Related Clinical Trials

Related PubMed Literature

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Official Source

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