Arthrotek, Inc. is one of 13825 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arthrotek, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE, 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS, HITCH LACTOSORB SUTURE ANCHOR
17
Total
17
Cleared
0
Denied
Arthrotek, Inc. has 17 FDA 510(k) cleared orthopedic devices. Based in West Hartford, US.
Historical record: 17 cleared submissions from 1987 to 2006.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arthrotek, Inc.
17 devices
Cleared
Sep 25, 2006
ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE
Orthopedic
94d
Cleared
Aug 07, 2006
2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS
Orthopedic
42d
Cleared
Jul 25, 2006
HITCH LACTOSORB SUTURE ANCHOR
Orthopedic
42d
Cleared
Jul 19, 2006
ALLTHREAD LACTOSORB SUTURE ANCHOR
Orthopedic
62d
Cleared
Jun 06, 2006
MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
Orthopedic
83d
Cleared
Feb 03, 2006
EZLOC FEMORAL FIXATION DEVICE
Orthopedic
52d
Cleared
Jun 29, 2005
NONRESORBABLE CENTRALOC TIBIAL SCREW & WASHER
Orthopedic
64d
Cleared
Oct 29, 2004
TI - SCREW ANCHOR SP
Orthopedic
49d
Cleared
Jul 28, 2004
RESORBABLE INTERFERENCE SCREW
Orthopedic
77d
Cleared
Jun 07, 2004
FEMORAL HOOK
Orthopedic
27d
Cleared
Jun 04, 2004
INNERVUE DIAGNOSTIC SCOPE SYSTEM
General & Plastic Surgery
88d
Cleared
May 25, 2004
ARTHROTEK LACTONAIL
Orthopedic
89d