FDA 510(k) Applications Submitted by ARTHROTEK, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K051069 04/26/2005 NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER ARTHROTEK, INC.
K041261 05/11/2004 FEMORAL HOOK ARTHROTEK, INC.
K041274 05/12/2004 RESORBABLE INTERFERENCE SCREW ARTHROTEK, INC.
K042460 09/10/2004 TI - SCREW ANCHOR SP ARTHROTEK, INC.
K040604 03/08/2004 INNERVUE DIAGNOSTIC SCOPE SYSTEM ARTHROTEK, INC.
K060693 03/15/2006 MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR ARTHROTEK, INC.
K061389 05/18/2006 ALLTHREAD LACTOSORB SUTURE ANCHOR ARTHROTEK, INC.
K061657 06/13/2006 HITCH LACTOSORB SUTURE ANCHOR ARTHROTEK, INC.
K061776 06/23/2006 ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE ARTHROTEK, INC.
K033718 11/26/2003 MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTURE ARTHROTEK, INC.
K012872 08/27/2001 RESORBABLE SCREW ANCHOR ARTHROTEK, INC.
K014305 12/31/2001 RESORBABLE LACTOSORB-L ACL CROSSPIN ARTHROTEK, INC.
K061801 06/26/2006 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS ARTHROTEK, INC.
K053461 12/13/2005 EZLOC FEMORAL FIXATION DEVICE ARTHROTEK, INC.
K040500 02/26/2004 ARTHROTEK LACTONAIL ARTHROTEK, INC.
K032072 07/03/2003 LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE ARTHROTEK, INC.


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