FDA 510(k) Applications Submitted by ARTIMPLANT AB

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040070	01/14/2004	ARTELON SPACER CMC-1	ARTIMPLANT AB
K052482	09/09/2005	ARTELON SURGICAL SUTURE	ARTIMPLANT AB
K032160	07/15/2003	ARTELON SURGICAL SUTURE	ARTIMPLANT AB
K061954	07/11/2006	ARTELON CMC SPACER ARTHRO	ARTIMPLANT AB
K061956	07/11/2006	ARTELON STT SPACER	ARTIMPLANT AB
K052830	10/05/2005	SPORTMESH	ARTIMPLANT AB
K071887	07/09/2007	SPORTMESH OR ARTELON TISSUE REINFORCEMENT	ARTIMPLANT AB