Artimplant AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K071887SPORTMESH OR ARTELON TISSUE REINFORCEMENTSeptember 18, 2007
K061956ARTELON STT SPACERJune 7, 2007
K061954ARTELON CMC SPACER ARTHROJune 1, 2007
K052830SPORTMESHJanuary 19, 2006
K052482ARTELON SURGICAL SUTUREOctober 17, 2005
K040070ARTELON SPACER CMC-1September 21, 2004
K032160ARTELON SURGICAL SUTURENovember 17, 2003