Intellijoint® Navigation System
K-Number: K191507 · 2019-10-01
Device Summary
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.
Related Devices (Code: OLO)
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.