meddevicedb.com FDA Device Reference

PlumeSafe X5 Smoke Management System

K240127 Class II Traditional
Decision Date
2024-08-05
Sponsor / Applicant
Conmed Corporation

Technical Specification

510(k) Submission ID K240127
Product Code FYD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 2024-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PlumeSafe X5 Smoke Management System received FDA 510(k) clearance under submission number K240127, sponsored by Conmed Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code FYD and 21 CFR 878.5070, within the General, Plastic Surgery review panel as a Class II device.