Arthrocare Corp. - FDA 510(k) Cleared Devices
Recent clearances: Adjustable Fixation Device, SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT, SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER OBTURATOR & SHARP TIPPED OBTURATOR, LOW PROFILE DR
112
Total
112
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrocare Corp. Orthopedic ✕
36 devices
Cleared
Jan 28, 2016
Adjustable Fixation Device
Orthopedic
86d
Cleared
Feb 27, 2013
SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER...
Orthopedic
30d
Cleared
Jul 20, 2011
SPEEDFIX SUTURE IMPLANT, 3.0MM DRILL, PATHFINDER OBTURATOR, SHARP TIPPED...
Orthopedic
62d
Cleared
Jul 12, 2011
TITAN TI SUTURE ANCHOR SYSTEM
Orthopedic
54d
Cleared
May 27, 2011
5.5 / 6.5MM SPARTAN PEEK SURTURE IMPLANT WITH #2 MAGNUMWIRE / WITH NEEDLES,...
Orthopedic
67d
Cleared
Feb 16, 2011
ARTHROCARE PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE
Orthopedic
26d
Cleared
Feb 07, 2011
5.5MM SPARTAN PEEK SUTURE IMPLANT W/ #2 MAGNUM WIRE, PUNCH TAP, EXTRACTION TOOL
Orthopedic
19d
Cleared
Oct 29, 2010
SPEEDFIX SUTURE SYSTEM
Orthopedic
158d
Cleared
Oct 21, 2010
ARTHOCARE SPARTAN PEEK SUTURE IMPLANT SYSTEM
Orthopedic
72d
Cleared
Sep 21, 2010
PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE
Orthopedic
215d
Cleared
Jun 21, 2010
OPUS SPEEDSCREW SYSTEM
Orthopedic
28d
Cleared
May 18, 2010
TITAN TI SUTURE ANCHOR SYSTEM, MODELS 22-9055, 22-9055N, 22-9065, 22-9065N,...
Orthopedic
20d