Arthrotek, Inc.
FDA 510(k) & PMA Approved Devices — 17 products
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Total Devices17
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061776 | ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE | JDR | 2006-09-25 | View |
| 510(k) | K061801 | 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS | JDR | 2006-08-07 | View |
| 510(k) | K061657 | HITCH LACTOSORB SUTURE ANCHOR | JDR | 2006-07-25 | View |
| 510(k) | K061389 | ALLTHREAD LACTOSORB SUTURE ANCHOR | JDR | 2006-07-19 | View |
| 510(k) | K060693 | MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR | HWC | 2006-06-06 | View |
| 510(k) | K053461 | EZLOC FEMORAL FIXATION DEVICE | MBI | 2006-02-03 | View |
| 510(k) | K051069 | NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER | MBI | 2005-06-29 | View |
| 510(k) | K042460 | TI - SCREW ANCHOR SP | MBI | 2004-10-29 | View |
| 510(k) | K041274 | RESORBABLE INTERFERENCE SCREW | HWC | 2004-07-28 | View |
| 510(k) | K041261 | FEMORAL HOOK | MBI | 2004-06-07 | View |
| 510(k) | K040604 | INNERVUE DIAGNOSTIC SCOPE SYSTEM | GCJ | 2004-06-04 | View |
| 510(k) | K040500 | ARTHROTEK LACTONAIL | HTY | 2004-05-25 | View |
| 510(k) | K033718 | MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTURE | GAT | 2004-02-12 | View |
| 510(k) | K032072 | LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE | HWC | 2003-10-01 | View |
| 510(k) | K014305 | RESORBABLE LACTOSORB-L ACL CROSSPIN | HTY | 2002-03-29 | View |
| 510(k) | K012872 | RESORBABLE SCREW ANCHOR | HWC | 2001-11-20 | View |
| 510(k) | K862286 | ARTHROPHONOMETER | NFQ | 1987-01-07 | View |
No matching devices.
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