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FDA 510(k)

SYMPHONY Navigation Ready Instruments

K-Number: K260240 · 2026-03-27

ApplicantMedos International SARL
Decision Date2026-03-27
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SYMPHONY Navigation Ready Instruments is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2026-03-27 under approval number K260240. 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 SYMPHONY Navigation Ready Instruments?

SYMPHONY Navigation Ready Instruments is a medical device that received FDA 510(k) clearance on 2026-03-27. It is manufactured by Medos International SARL. The 510(k) number is K260240.

When was SYMPHONY Navigation Ready Instruments approved by the FDA?

SYMPHONY Navigation Ready Instruments received FDA 510(k) clearance on 2026-03-27, under approval number K260240.

What company makes SYMPHONY Navigation Ready Instruments?

SYMPHONY Navigation Ready Instruments is manufactured by Medos International SARL.

What is the FDA product code for SYMPHONY Navigation Ready Instruments?

The FDA product code for SYMPHONY Navigation Ready 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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