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Extremity Medical External Fixation System

K241563 Class II Traditional
Decision Date
2025-02-21
Sponsor / Applicant
Extremity Medical, LLC

Technical Specification

510(k) Submission ID K241563
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2025-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Extremity Medical External Fixation System received FDA 510(k) clearance under submission number K241563, sponsored by Extremity Medical, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code KTT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.