Novopore Dressing

FDA 510(k) K132936 · Polynovo Biomaterials Pty, Ltd.

Substantially Equivalent

510(k) numberK132936

Submission

Device name
Novopore Dressing
Applicant
Polynovo Biomaterials Pty, Ltd.
Austin, TX, US
Received
September 18, 2013
Decision date
March 4, 2014
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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K172140NovoSorb BTM Wound Dressing (2cm x 2cm), NovoSorb BTM Wound Dressing (10cm x 10cm)…QSZ · Special 08/11/2017SE
K142879BTM Wound DressingQSZ · Traditional 12/23/2015SE

Questions and answers

When was Novopore Dressing cleared by the FDA?

Novopore Dressing (K132936) received a 510(k) decision of Substantially Equivalent on March 4, 2014, 167 days after the submission was received.

What is the product code of K132936?

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.