Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments)
K-Number: K251073 · 2025-07-23
Device Summary
Frequently Asked Questions
What is the Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments)?
Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments) is a medical device that received FDA 510(k) clearance on 2025-07-23. It is manufactured by Innovasis, Inc.. The 510(k) number is K251073.
When was Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments) approved by the FDA?
Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments) received FDA 510(k) clearance on 2025-07-23, under approval number K251073.
What company makes Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments)?
Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments) is manufactured by Innovasis, Inc..
What is the FDA product code for Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments)?
The FDA product code for Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments) is OLO.
Related Clinical Trials
Other Devices by Innovasis, 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.