Arthrotek, Inc.
Arthrotek, Inc. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 25, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 17
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K061776 | ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE | Sep 25, 2006 |
| K061801 | 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS | Aug 7, 2006 |
| K061657 | HITCH LACTOSORB SUTURE ANCHOR | Jul 25, 2006 |
| K061389 | ALLTHREAD LACTOSORB SUTURE ANCHOR | Jul 19, 2006 |
| K060693 | MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR | Jun 6, 2006 |
| K053461 | EZLOC FEMORAL FIXATION DEVICE | Feb 3, 2006 |
| K051069 | NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER | Jun 29, 2005 |
| K042460 | TI - SCREW ANCHOR SP | Oct 29, 2004 |
| K041274 | RESORBABLE INTERFERENCE SCREW | Jul 28, 2004 |
| K041261 | FEMORAL HOOK | Jun 7, 2004 |
| K040604 | INNERVUE DIAGNOSTIC SCOPE SYSTEM | Jun 4, 2004 |
| K040500 | ARTHROTEK LACTONAIL | May 25, 2004 |
| K033718 | MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTURE | Feb 12, 2004 |
| K032072 | LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE | Oct 1, 2003 |
| K014305 | RESORBABLE LACTOSORB-L ACL CROSSPIN | Mar 29, 2002 |
| K012872 | RESORBABLE SCREW ANCHOR | Nov 20, 2001 |
| K862286 | ARTHROPHONOMETER | Jan 7, 1987 |