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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