Home » ANULEX TECHNOLOGIES RECEIVES FDA 510(K) CLEARANCE FOR THE INCLOSE SURGICAL MESH SYSTEM
ANULEX TECHNOLOGIES RECEIVES FDA 510(K) CLEARANCE FOR THE INCLOSE SURGICAL MESH SYSTEM
Anulex Technologies, Inc. announced today that it has received FDA 510(k) clearance of its Inclose(TM) Surgical Mesh System. The Inclose(TM) Surgical Mesh System is a novel, patented implant that is designed to provide a barrier and scaffold to facilitate the repair of soft tissue. The surgical mesh implant is comprised of polyethylene terephthalate (PET) monofilament braid material that is preloaded on a disposable delivery tool.
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(http://minneapolis.dbusinessnews.com/shownews.php?newsid=40918&type_news=latest)
KEYWORDS FDAnews Device Daily Bulletin
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