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Arthrotek, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061776ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICESeptember 25, 2006
K0618012.8 & 3.5MM LACTOSCREW SUTURE ANCHORSAugust 7, 2006
K061657HITCH LACTOSORB SUTURE ANCHORJuly 25, 2006
K061389ALLTHREAD LACTOSORB SUTURE ANCHORJuly 19, 2006
K060693MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHORJune 6, 2006
K053461EZLOC FEMORAL FIXATION DEVICEFebruary 3, 2006
K051069NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHERJune 29, 2005
K042460TI - SCREW ANCHOR SPOctober 29, 2004
K041274RESORBABLE INTERFERENCE SCREWJuly 28, 2004
K041261FEMORAL HOOKJune 7, 2004
K040604INNERVUE DIAGNOSTIC SCOPE SYSTEMJune 4, 2004
K040500ARTHROTEK LACTONAILMay 25, 2004
K033718MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTUREFebruary 12, 2004
K032072LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTUREOctober 1, 2003
K014305RESORBABLE LACTOSORB-L ACL CROSSPINMarch 29, 2002
K012872RESORBABLE SCREW ANCHORNovember 20, 2001
K862286ARTHROPHONOMETERJanuary 7, 1987