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mb-FIX Cranial Stabilization Systems

K250423 Class II Traditional
Decision Date
2025-11-06
Sponsor / Applicant
Medical Bees GmbH

Technical Specification

510(k) Submission ID K250423
Product Code HBL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4460
Decision Date 2025-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

mb-FIX Cranial Stabilization Systems received FDA 510(k) clearance under submission number K250423, sponsored by Medical Bees GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2025-11-06.

Classification & Regulation

This clearance is catalogued under FDA product code HBL and 21 CFR 882.4460, within the Neurology review panel as a Class II device.