Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
31 to 40 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
Results per Page
New Search  
Export all 68 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
arthrocare system ARTHROCARE CORP. K032504 08/21/2003
arthrocare percd spinewand ARTHROCARE CORP. K030954 04/16/2003
arthrocare controller (system 2000 and 8000); arthrocare patient cable; foot control; power cord; wands ARTHROCARE CORP. K030551 03/07/2003
arthrocare ent coblator surgery system ARTHROCARE CORP. K030108 02/03/2003
modification to arthrocare controller (system 2000 and 8000), arthrocare patient cable, foot control, power cord, wands ARTHROCARE CORP. K022475 10/03/2002
arthrocare controller, authrocare cable, foot control, power cord, wands ARTHROCARE CORP. K021519 06/06/2002
modification to entec plasma wands ARTHROCARE CORP. K021364 05/30/2002
system 2000 controller, system 5000 controller, footswitch, power cord, and visage wandsff ARTHROCARE CORP. K020408 05/02/2002
arthrocare controller, arthrocare cable, foot control, power cord, wands ARTHROCARE CORP. K020832 04/09/2002
arthrocare controller (system 2000 and 8000); arthrocare cable; foot control; power cord; and wands ARTHROCARE CORP. K020622 03/28/2002
-
-