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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 the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2026-03-27 under 510(k) 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. The listed applicant is Medos International SARL. The 510(k) number is K260240.

When did SYMPHONY Navigation Ready Instruments receive FDA 510(k) clearance?

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

Who is the listed applicant for SYMPHONY Navigation Ready Instruments?

The FDA 510(k) record lists Medos International SARL as the applicant. This does not by itself establish the device manufacturer.

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

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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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