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
-
1 to 10 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]
arthocare arthroscopic electrosurgery system model 970 ARTHROCARE CORP. K962321 07/19/1996
arthrocare 8000s coblator surgery system ARTHROCARE CORP. K053297 12/06/2005
arthrocare arthro wands, enetec evac plasma wand ARTHROCARE CORP. K013463 11/15/2001
arthrocare arthroscopic eletrosurgery system (model 980) ARTHROCARE CORP. K963123 10/08/1996
arthrocare arthrowands ARTHROCARE CORP. K033584 11/28/2003
arthrocare arthrowands ARTHROCARE CORP. K052686 10/05/2005
arthrocare arthrowands ARTHROCARE CORP. K082323 08/28/2008
arthrocare arthrowands ARTHROCARE CORP. K082980 11/05/2008
arthrocare cavity spinewand ARTHROCARE CORP. K063172 04/27/2007
arthrocare coblator iq system ARTHROCARE CORP. K091674 01/15/2010
-
-