Dallen Medical Files 510(k) for FDA Clearance on Sterile Packaging for Compressyn Staple Implants
Published: Sep 17, 2013
SAN CLEMENTE, Calif.--(BUSINESS WIRE)--Dallen Medical has filed its FDA 510(k) application for individually packaged, sterile Compressyn™ staple implants. Clearance of the Compressyn staple was already received in February of this year as a reusable system for small bone fixation, specifically in foot, ankle and hand applications. With three FDA clearances already received, this continues the company’s plan to expand its Compressyn family of products.
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