meddevicedb.com FDA Device Reference

External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters

K242974 Class II Traditional
Decision Date
2025-06-20
Sponsor / Applicant
Sophysa

Technical Specification

510(k) Submission ID K242974
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 2025-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters received FDA 510(k) clearance under submission number K242974, sponsored by Sophysa. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2025-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code JXG and 21 CFR 882.5550, within the Neurology review panel as a Class II device.