Renasys Ez Max Negative Pressure Wound Therapy Device

FDA 510(k) K132446 · Smith & Nephew, Inc.

Substantially Equivalent

510(k) numberK132446

Submission

Device name
Renasys Ez Max Negative Pressure Wound Therapy Device
Applicant
Smith & Nephew, Inc.
St Petersburg, FL, US
Received
August 6, 2013
Decision date
October 23, 2013
Decision
Substantially Equivalent (SESE)
Type
Special 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 Renasys Ez Max Negative Pressure Wound Therapy Device cleared by the FDA?

Renasys Ez Max Negative Pressure Wound Therapy Device (K132446) received a 510(k) decision of Substantially Equivalent on October 23, 2013, 78 days after the submission was received.

What is the product code of K132446?

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.