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FDA 510(k)

Intellijoint® Navigation System

K-Number: K191507 · 2019-10-01

Decision Date2019-10-01
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Intellijoint® Navigation System is a medical device manufactured by Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2019-10-01 under approval number K191507. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intellijoint® Navigation System?

Intellijoint® Navigation System is a medical device that received FDA 510(k) clearance on 2019-10-01. It is manufactured by Intellijoint Surgical, Inc.. The 510(k) number is K191507.

When was Intellijoint® Navigation System approved by the FDA?

Intellijoint® Navigation System received FDA 510(k) clearance on 2019-10-01, under approval number K191507.

What company makes Intellijoint® Navigation System?

Intellijoint® Navigation System is manufactured by Intellijoint Surgical, Inc..

What is the FDA product code for Intellijoint® Navigation System?

The FDA product code for Intellijoint® Navigation System is OLO.

Related Clinical Trials

Related PubMed Literature

Other Devices by Intellijoint Surgical, Inc.

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Official Source

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