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ABTHERA OPEN ABDOMEN NEGATIVE PRESSURE THERAPY SYSTEM

K120499 Class II Traditional
Decision Date
2012-10-05
Sponsor / Applicant
Kci USA, Inc. (Kinetic Concepts, Inc.)

Technical Specification

510(k) Submission ID K120499
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2012-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABTHERA OPEN ABDOMEN NEGATIVE PRESSURE THERAPY SYSTEM received FDA 510(k) clearance under submission number K120499, sponsored by Kci USA, Inc. (Kinetic Concepts, Inc.). 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 2012-10-05.

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.