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Artimplant AB

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K071887	SPORTMESH OR ARTELON TISSUE REINFORCEMENT	FTL	2007-09-18	View
510(k)	K061956	ARTELON STT SPACER	KYI	2007-06-07	View
510(k)	K061954	ARTELON CMC SPACER ARTHRO	KYI	2007-06-01	View
510(k)	K052830	SPORTMESH	FTL	2006-01-19	View
510(k)	K052482	ARTELON SURGICAL SUTURE	GAR	2005-10-17	View
510(k)	K040070	ARTELON SPACER CMC-1	KYI	2004-09-21	View
510(k)	K032160	ARTELON SURGICAL SUTURE	GAR	2003-11-17	View

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