Revolution Spinal Fixation System
K-Number: K160216 · 2016-04-22
Device Summary
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. The listed applicant is Intelligent Implant Systems, LLC. The 510(k) number is K160216.
When did Revolution Spinal Fixation System receive FDA 510(k) clearance?
Revolution Spinal Fixation System received FDA 510(k) clearance on 2016-04-22, under 510(k) number K160216.
Who is the listed applicant for Revolution Spinal Fixation System?
The FDA 510(k) record lists Intelligent Implant Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Revolution Spinal Fixation System?
The FDA product code for Revolution Spinal Fixation System is NKB.
Other records listing Intelligent Implant Systems, LLC 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.