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FDA 510(k)

Medusa Orthopedics Boa External Fixation System

K-Number: K252555 · 2025-11-25

ApplicantMedusa Orthopedics, LLC
Decision Date2025-11-25
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Medusa Orthopedics Boa External Fixation System is a medical device manufactured by Medusa Orthopedics, LLC. It received FDA 510(k) clearance on 2025-11-25 under approval number K252555. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medusa Orthopedics Boa External Fixation System?

Medusa Orthopedics Boa External Fixation System is a medical device that received FDA 510(k) clearance on 2025-11-25. It is manufactured by Medusa Orthopedics, LLC. The 510(k) number is K252555.

When was Medusa Orthopedics Boa External Fixation System approved by the FDA?

Medusa Orthopedics Boa External Fixation System received FDA 510(k) clearance on 2025-11-25, under approval number K252555.

What company makes Medusa Orthopedics Boa External Fixation System?

Medusa Orthopedics Boa External Fixation System is manufactured by Medusa Orthopedics, LLC.

What is the FDA product code for Medusa Orthopedics Boa External Fixation System?

The FDA product code for Medusa Orthopedics Boa External Fixation System is KTT.

Related Clinical Trials

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Related Devices (Code: KTT)

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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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