Company ยท US
Arthrotek, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 2006. Name variants (Inc, Corp, punctuation) are merged.
17510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 25, 2006 | K061776 | ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE Arthrotek, Inc. | JDR |
| Aug 7, 2006 | K061801 | 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS Arthrotek, Inc. | JDR |
| Jul 25, 2006 | K061657 | HITCH LACTOSORB SUTURE ANCHOR Arthrotek, Inc. | JDR |
| Jul 19, 2006 | K061389 | ALLTHREAD LACTOSORB SUTURE ANCHOR Arthrotek, Inc. | JDR |
| Jun 6, 2006 | K060693 | MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR Arthrotek, Inc. | HWC |
| Feb 3, 2006 | K053461 | EZLOC FEMORAL FIXATION DEVICE Arthrotek, Inc. | MBI |
| Jun 29, 2005 | K051069 | NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER Arthrotek, Inc. | MBI |
| Oct 29, 2004 | K042460 | TI - SCREW ANCHOR SP Arthrotek, Inc. | MBI |
| Jul 28, 2004 | K041274 | RESORBABLE INTERFERENCE SCREW Arthrotek, Inc. | HWC |
| Jun 7, 2004 | K041261 | FEMORAL HOOK Arthrotek, Inc. | MBI |
| Jun 4, 2004 | K040604 | INNERVUE DIAGNOSTIC SCOPE SYSTEM Arthrotek, Inc. | GCJ |
| May 25, 2004 | K040500 | ARTHROTEK LACTONAIL Arthrotek, Inc. | HTY |
| Feb 12, 2004 | K033718 | MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTURE Arthrotek, Inc. | GAT |
| Oct 1, 2003 | K032072 | LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE Arthrotek, Inc. | HWC |
| Mar 29, 2002 | K014305 | RESORBABLE LACTOSORB-L ACL CROSSPIN Arthrotek, Inc. | HTY |
| Nov 20, 2001 | K012872 | RESORBABLE SCREW ANCHOR Arthrotek, Inc. | HWC |
| Jan 7, 1987 | K862286 | ARTHROPHONOMETER Arthrotek, Inc. | NFQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||