Cleared Traditional

K021501 - V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT
(FDA 510(k) Clearance)

K021501 · Kinetic Concepts, Inc. · General & Plastic Surgery
Dec 2002
Decision
207d
Days
Class 2
Risk

K021501 is an FDA 510(k) clearance for the V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT. This device is classified as a Negative Pressure Wound Therapy Powered Suction Pump (Class II — Special Controls, product code OMP).

Submitted by Kinetic Concepts, Inc. (San Antonio, US). The FDA issued a Cleared decision on December 2, 2002, 207 days after receiving the submission on May 9, 2002.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4780. 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..

Submission Details

510(k) Number K021501 FDA.gov
FDA Decision Cleared SESE
Date Received May 09, 2002
Decision Date December 02, 2002
Days to Decision 207 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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