Cleared Traditional

Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100)

K243187 · Cork Medical · General & Plastic Surgery
Jun 2025
Decision
270d
Days
Class 2
Risk

About This 510(k) Submission

K243187 is an FDA 510(k) clearance for the Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100), a Negative Pressure Wound Therapy Powered Suction Pump (Class II — Special Controls, product code OMP), submitted by Cork Medical (Indianapolis, US). The FDA issued a Cleared decision on June 27, 2025, 270 days after receiving the submission on September 30, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4780.

Submission Details

510(k) Number K243187 FDA.gov
FDA Decision Cleared SESE
Date Received September 30, 2024
Decision Date June 27, 2025
Days to Decision 270 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OMP — Negative Pressure Wound Therapy Powered Suction Pump
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4780
Definition 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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