ArthroCare Corporation - FDA 510(k) Cleared Devices
Recent clearances: LYNX COBLATION Laryngeal Wand (72290254), FLOW 90? Wand, INTELLIO SHIFT System
36
Total
36
Cleared
0
Denied
FDA 510(k) Regulatory Record - ArthroCare Corporation Orthopedic ✕
13 devices
Cleared
Aug 17, 2017
Q-Fix Suture Anchor
Orthopedic
30d
Cleared
Dec 11, 2015
SpeedLock Knotless Fixation System
Orthopedic
24d
Cleared
Aug 06, 2015
MultiFIX® P Knotless Fixation Device
Orthopedic
27d
Cleared
Jul 16, 2015
MultiFIX S Knotless Fixation System
Orthopedic
27d
Cleared
May 14, 2014
MULTIFIX S KNOTLESS FIXATION SYSTEM
Orthopedic
65d
Cleared
Apr 01, 2014
N8TIVE ACL ANATOMIC RECONSTRUCTION SYSTEM, N8TIVE ACL FEMORAL IMPLANT, N8TIVE...
Orthopedic
127d
Cleared
Jan 16, 2014
Q-FIX SUTURE ANCHOR, 1.8MM
Orthopedic
41d
Cleared
Sep 19, 2013
Q-FIX SUTURE ANCHOR,1.8MM AND 2.8MM / DRILL, DRILL GUIDE AND OBTURATOR,1.8MM...
Orthopedic
38d
Cleared
Sep 17, 2013
5.5MM MULTIFIX S KNOTLESS FIXATION DEVICE, 6.5MM MULTIFIX S KNOTLESS FIXATION...
Orthopedic
29d
Cleared
Feb 14, 2013
SPEEDLOCK HIP KNOTLESS FIXATION IMPLANT
Orthopedic
121d
Cleared
Sep 21, 2012
SPEEDLOCK HIP KNOTLESS FIXATION IMPLANT SPEEDLOCK HIP DRILL SPEEDLOCK HIP...
Orthopedic
176d
Cleared
Mar 27, 2012
MULTIFIX P KNOTLESS FIXATION DEVICE
Orthopedic
75d