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FDA 510(k)

Excella Navigation Instruments

K-Number: K223511 · 2023-05-02

ApplicantInnovasis, Inc.
Decision Date2023-05-02
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Excella Navigation Instruments is a medical device manufactured by Innovasis, Inc.. It received FDA 510(k) clearance on 2023-05-02 under approval number K223511. 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 Excella Navigation Instruments?

Excella Navigation Instruments is a medical device that received FDA 510(k) clearance on 2023-05-02. It is manufactured by Innovasis, Inc.. The 510(k) number is K223511.

When was Excella Navigation Instruments approved by the FDA?

Excella Navigation Instruments received FDA 510(k) clearance on 2023-05-02, under approval number K223511.

What company makes Excella Navigation Instruments?

Excella Navigation Instruments is manufactured by Innovasis, Inc..

What is the FDA product code for Excella Navigation Instruments?

The FDA product code for Excella Navigation Instruments is OLO.

Related Clinical Trials

NCT07518615 Clinical Safety and Effectiveness of the Straumann Dynamic Navigation System Falcon RECRUITING

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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.

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