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Arthrotek, Inc.

17 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE (K061776)Arthrotek, Inc.2006-09-25
2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS (K061801)Arthrotek, Inc.2006-08-07
HITCH LACTOSORB SUTURE ANCHOR (K061657)Arthrotek, Inc.2006-07-25
ALLTHREAD LACTOSORB SUTURE ANCHOR (K061389)Arthrotek, Inc.2006-07-19
MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR (K060693)Arthrotek, Inc.2006-06-06
EZLOC FEMORAL FIXATION DEVICE (K053461)Arthrotek, Inc.2006-02-03
NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER (K051069)Arthrotek, Inc.2005-06-29
TI - SCREW ANCHOR SP (K042460)Arthrotek, Inc.2004-10-29
RESORBABLE INTERFERENCE SCREW (K041274)Arthrotek, Inc.2004-07-28
FEMORAL HOOK (K041261)Arthrotek, Inc.2004-06-07
INNERVUE DIAGNOSTIC SCOPE SYSTEM (K040604)Arthrotek, Inc.2004-06-04
ARTHROTEK LACTONAIL (K040500)Arthrotek, Inc.2004-05-25
MAXBRAID POLYESTER PLUS AND POLYETHYLENE PLUS SUTURE (K033718)Arthrotek, Inc.2004-02-12
LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE (K032072)Arthrotek, Inc.2003-10-01
RESORBABLE LACTOSORB-L ACL CROSSPIN (K014305)Arthrotek, Inc.2002-03-29
RESORBABLE SCREW ANCHOR (K012872)Arthrotek, Inc.2001-11-20
ARTHROPHONOMETER (K862286)Arthrotek, Inc.1987-01-07

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Every clearance here is in the API, with alerts when new ones post.