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. General & Plastic Surgery ✕
65 devices
Cleared
May 13, 2010
SPINEWAND SURGICAL DEVICE
General & Plastic Surgery
90d
Cleared
Jan 15, 2010
ARTHROCARE COBLATOR IQ SYSTEM
General & Plastic Surgery
220d
Cleared
Dec 04, 2009
ARTHROCARE SYSTEM 15000 CONTROLLER, ARTHROWANDS
General & Plastic Surgery
59d
Cleared
Sep 28, 2009
SPINEWAND SURGICAL DEVICE
General & Plastic Surgery
154d
Cleared
Jun 23, 2009
ARTHROCARE SYSTEM 15000 CONTOLLER, MODEL 72202149, ARTHROCARE ARTHROWANDS,...
General & Plastic Surgery
126d
Cleared
Dec 10, 2008
MODIFICATION TO ARTHROCARE ARTHROWANDS
General & Plastic Surgery
30d
Cleared
Nov 05, 2008
ARTHROCARE ARTHROWANDS
General & Plastic Surgery
30d
Cleared
Oct 15, 2008
ARTHROCARE CONTROLLER (SYSTEM 12000), ARTHROCARE PATIENT CABLE, FOOT CONTROL,...
General & Plastic Surgery
33d
Cleared
Aug 28, 2008
ARTHROCARE ARTHROWANDS
General & Plastic Surgery
14d
Cleared
Mar 31, 2008
ARTHROCARE ORTHOWAND SURGICAL DEVICE
General & Plastic Surgery
27d
Cleared
Mar 20, 2008
ARTHROCARE IRRIGATION PUMP, MODEL SIP001-00, SIP001-01
General & Plastic Surgery
27d
Cleared
Feb 15, 2008
ARTHROCARE CONTROLLERS (SYSTEM 2000,1100,1200), MODEL H2076-00, H2079-00,...
General & Plastic Surgery
11d
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