Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Pytheas Navigation Sas. It received FDA 510(k) clearance on 2026-05-11 under 510(k) 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. The listed applicant is Pytheas Navigation Sas. The 510(k) number is K252880.

When did Pytheas Your Guided Trajectory receive FDA 510(k) clearance?

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

Who is the listed applicant for Pytheas Your Guided Trajectory?

The FDA 510(k) record lists Pytheas Navigation Sas as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: OLO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261410Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration Kit))Suite 201, National Innovation CentreK261205SPINEART Navigation Instrument SystemSpineart SAK262121Ion-L Navigated InstrumentsSurGenTec, LLCK261024TMINI Miniature Robotic SystemTHINK Surgical, Inc.K261113Op.n™ Spine Navigation and Robotic GuidanceEcential RoboticsK261852OTS HipOrtoma AB

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.

↑