FDA Issues 510(k) Clearance to Applied Tissue Technologies’ Platform Wound Dressing (PWD®), A New Negative Pressure Wound Therapy System Without Foam or Gauze - Applied Tissue Technologies - Complete Wound Care

FDA Issues 510(k) Clearance to Applied Tissue Technologies’ Platform Wound Dressing (PWD®), A New Negative Pressure Wound Therapy System Without Foam or Gauze

Post author:appliedtissue
Post published:January 15, 2019
Post category:Uncategorized

Applied Tissue Technologies (ATT), an advanced wound care company, announced US FDA 510(k) clearance of its Negative Pressure Wound Therapy product, the Platform Wound Dressing (PWD®). Classified by the FDA as a class II device, the patented PWD represents the first-of-its-kind embossed negative pressure wound therapy (NPWT) device to be used without foam or gauze.