meddevicedb.com FDA Device Reference

V.A.C.ULTA Negative Pressure Wound Therapy System

K203316 Class II Traditional
Decision Date
2021-10-27
Sponsor / Applicant
Kci, A Part of 3M Health Care Business Group

Technical Specification

510(k) Submission ID K203316
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2021-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V.A.C.ULTA Negative Pressure Wound Therapy System received FDA 510(k) clearance under submission number K203316, sponsored by Kci, A Part of 3M Health Care Business Group. 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 2021-10-27.

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.