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FDA 510(k)

CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays

K-Number: K241893 · 2024-09-16

ApplicantMedos International SARL
Decision Date2024-09-16
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2024-09-16 under approval number K241893. 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 CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays?

CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays is a medical device that received FDA 510(k) clearance on 2024-09-16. It is manufactured by Medos International SARL. The 510(k) number is K241893.

When was CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays approved by the FDA?

CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays received FDA 510(k) clearance on 2024-09-16, under approval number K241893.

What company makes CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays?

CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays is manufactured by Medos International SARL.

What is the FDA product code for CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays?

The FDA product code for CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays is OLO.

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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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