meddevicedb.com FDA Device Reference

Avance Solo Negative Pressure Wound Therapy (NPWT) System

K203369 Class II Traditional
Decision Date
2021-07-01
Sponsor / Applicant
Molnlycke Health Care Us, LLC

Technical Specification

510(k) Submission ID K203369
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2021-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Avance Solo Negative Pressure Wound Therapy (NPWT) System received FDA 510(k) clearance under submission number K203369, sponsored by Molnlycke Health Care Us, LLC. 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 2021-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.