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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 112 Results
Applicant: ARTHROCARE CORP. Decision Date To: 05/02/2024
 
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510(K)
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adjustable fixation device ARTHROCARE CORP. K153186 01/28/2016
sinus dilation system with cannulated instrument ARTHROCARE CORP. K131709 10/04/2013
speedlock knotless fixation device, 3mm drill, 3mm+ drill, pathfinder obturator & sharp tipped obturator, low profile dr ARTHROCARE CORP. K130196 02/27/2013
speedfix suture implant, 3.0mm drill, pathfinder obturator, sharp tipped obtrurator, low profile drill guide model om-75 ARTHROCARE CORP. K111399 07/20/2011
titan ti suture anchor system ARTHROCARE CORP. K111397 07/12/2011
5.5 / 6.5mm spartan peek surture implant with #2 magnumwire / with needles, extraction tool, 5.5 / 6.5mm punch tap ARTHROCARE CORP. K110781 05/27/2011
arthrocare parallax contour vertebral augmentation device ARTHROCARE CORP. K110183 02/16/2011
5.5mm spartan peek suture implant w/ #2 magnum wire, punch tap, extraction tool ARTHROCARE CORP. K110164 02/07/2011
speedfix suture system ARTHROCARE CORP. K101437 10/29/2010
arthocare spartan peek suture implant system; punch tap ; extraction tool ARTHROCARE CORP. K102262 10/21/2010
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