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Arthrocare Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
112
Inspections
3
Compliance Actions
0

Known Names

arthrocare corporation, arthrocare

Recent 510(k) Clearances

K-NumberDeviceDate
K153186Adjustable Fixation DeviceJanuary 28, 2016
K131709SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENTOctober 4, 2013
K130196SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER OBTURATOR & SHARP TIPPED OBTURFebruary 27, 2013
K111399SPEEDFIX SUTURE IMPLANT, 3.0MM DRILL, PATHFINDER OBTURATOR, SHARP TIPPED OBTRURATOR, LOW PROFILE DRIJuly 20, 2011
K111397TITAN TI SUTURE ANCHOR SYSTEMJuly 12, 2011
K1107815.5 / 6.5MM SPARTAN PEEK SURTURE IMPLANT WITH #2 MAGNUMWIRE / WITH NEEDLES, EXTRACTION TOOL, 5.5 / 6May 27, 2011
K110183ARTHROCARE PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICEFebruary 16, 2011
K1101645.5MM SPARTAN PEEK SUTURE IMPLANT W/ #2 MAGNUM WIRE, PUNCH TAP, EXTRACTION TOOLFebruary 7, 2011
K101437SPEEDFIX SUTURE SYSTEMOctober 29, 2010
K102262ARTHOCARE SPARTAN PEEK SUTURE IMPLANT SYSTEM; PUNCH TAP ; EXTRACTION TOOLOctober 21, 2010
K100479PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICESeptember 21, 2010
K101448OPUS SPEEDSCREW SYSTEMJune 21, 2010
K101184TITAN TI SUTURE ANCHOR SYSTEM, MODELS 22-9055, 22-9055N, 22-9065, 22-9065N, 22-9022, 22-9005,, 22-90May 18, 2010
K100353SPINEWAND SURGICAL DEVICEMay 13, 2010
K100457OPUS SPEEDSCREW SYSTEMMarch 19, 2010
K091674ARTHROCARE COBLATOR IQ SYSTEMJanuary 15, 2010
K093165ARTHROCARE SYSTEM 15000 CONTROLLER, ARTHROWANDSDecember 4, 2009
K092133ARTHROCARE TITANIUM SUTURE ANCHOR, MODEL 22-9055,22-9055N, 22-9065, 22-9065NNovember 5, 2009
K091228SPINEWAND SURGICAL DEVICESeptember 28, 2009
K090393ARTHROCARE SYSTEM 15000 CONTOLLER, MODEL 72202149, ARTHROCARE ARTHROWANDS, MODEL 72202139,72202141, June 23, 2009