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FDA 510(k)

Pytheas Your Guided Trajectory

K-Number: K252880 · 2026-05-11

ApplicantPytheas Navigation Sas
Decision Date2026-05-11
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Pytheas Your Guided Trajectory is a medical device manufactured by Pytheas Navigation Sas. It received FDA 510(k) clearance on 2026-05-11 under approval number K252880. 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 Pytheas Your Guided Trajectory?

Pytheas Your Guided Trajectory is a medical device that received FDA 510(k) clearance on 2026-05-11. It is manufactured by Pytheas Navigation Sas. The 510(k) number is K252880.

When was Pytheas Your Guided Trajectory approved by the FDA?

Pytheas Your Guided Trajectory received FDA 510(k) clearance on 2026-05-11, under approval number K252880.

What company makes Pytheas Your Guided Trajectory?

Pytheas Your Guided Trajectory is manufactured by Pytheas Navigation Sas.

What is the FDA product code for Pytheas Your Guided Trajectory?

The FDA product code for Pytheas Your Guided Trajectory is OLO.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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