Arthrotek, Inc.
Arthrotek, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2006.
Top product codes for Arthrotek, Inc.
Recent clearances by Arthrotek, Inc.
- K061776 — ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE
- K061801 — 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS
- K061657 — HITCH LACTOSORB SUTURE ANCHOR
- K061389 — ALLTHREAD LACTOSORB SUTURE ANCHOR
- K060693 — MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
- K053461 — EZLOC FEMORAL FIXATION DEVICE
- K051069 — NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER
- K042460 — TI - SCREW ANCHOR SP
- K041274 — RESORBABLE INTERFERENCE SCREW
- K041261 — FEMORAL HOOK
- K040604 — INNERVUE DIAGNOSTIC SCOPE SYSTEM
- K040500 — ARTHROTEK LACTONAIL
- K033718 — MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTURE
- K032072 — LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE
- K014305 — RESORBABLE LACTOSORB-L ACL CROSSPIN
- K012872 — RESORBABLE SCREW ANCHOR
- K862286 — ARTHROPHONOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.