AVELLE Negative Pressure Wound Therapy System

FDA 510(k) K180205 · Convatec Limited

Substantially Equivalent

510(k) numberK180205

Submission

Device name
AVELLE Negative Pressure Wound Therapy System
Applicant
Convatec Limited
Deeside, GB
Received
January 24, 2018
Decision date
October 19, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OMP – Negative Pressure Wound Therapy Powered Suction Pump
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

For wound management via application of continual or intermittent negative pressure to the wound for removal of fluids, including wound exudate, irrigation fluids, and infectious materials. The Device is indicated for management of chronic, acute, traumatic, subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts.

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Questions and answers

When was AVELLE Negative Pressure Wound Therapy System cleared by the FDA?

AVELLE Negative Pressure Wound Therapy System (K180205) received a 510(k) decision of Substantially Equivalent on October 19, 2018, 268 days after the submission was received.

What is the product code of K180205?

The FDA product code is OMP – Negative Pressure Wound Therapy Powered Suction Pump, a Class II (moderate risk) device regulated under 21 CFR 878.4780.