VANCOUVER, Feb. 26 /PRNewswire-FirstCall/ - Angiotech Pharmaceuticals, Inc. (NASDAQ: ANPI; TSX: ANP), a global specialty pharmaceutical and medical device company, today announced that it has received 510(k) clearance to begin marketing the Quill(TM) SRS Polydioxanone (PDO), MONODERM(TM) and Nylon product lines in Canada.
"With the approval of the PDO, MONODERM(TM) and Nylon product lines in Canada, we can further extend the global reach of this next-generation suture product beyond the U.S. and Europe," said Dr. William Hunter, President and CEO of Angiotech.
Quill(TM) SRS PDO is a longer-lasting absorbable suture, which is typically used for deeper tissue closures while Quill(TM) SRS MONODERM(TM) is made from a rapidly resorbing polymer and intended primarily for superficial wound closure applications and soft tissue approximation where use of an absorbable suture is appropriate. The monofilament Quill(TM) SRS Nylon is a polyamide suture indicated for use in soft tissue approximation excluding closure of the epidermis.
Quill(TM) SRS PDO, MONODERM(TM) and Nylon product lines have both been previously approved for sale in the U.S. and Europe.
About the Quill(TM) Self-Retaining System (SRS)
Quill(TM) SRS represents a revolutionary technology in wound closure made possible by bidirectional fixation within the wound. Its patented design allows the surgeon to begin closure at the midpoint of the wound and suture in two directions from the midpoint. Barbs within the Quill(TM) SRS distribute tension across the wound and eliminate the need for knots.
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|SOURCE Angiotech Pharmaceuticals, Inc.|
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