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ABTHERA OPEN ABDOMEN DRESSING, MODEL: M8275026

K090489 Class II Special
Decision Date
2009-05-14
Sponsor / Applicant
Kci USA, Inc.

Technical Specification

510(k) Submission ID K090489
Product Code FTL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2009-05-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABTHERA OPEN ABDOMEN DRESSING, MODEL: M8275026 received FDA 510(k) clearance under submission number K090489, sponsored by Kci USA, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2009-05-14.

Classification & Regulation

This clearance is catalogued under FDA product code FTL and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.