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 24 Results
ProductCode: HRS Applicant: ARTHREX, INC. Decision Date To: 01/28/2022
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 24 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]
opening/closing wedge ostetomy plates ARTHREX, INC. K014155 03/18/2002
low profile screws ARTHREX, INC. K103705 03/18/2011
low profile plate and screw system ARTHREX, INC. K052614 09/28/2005
arthrex tensionlok ARTHREX, INC. K052901 12/12/2005
arthrex small fragment plates and screws ARTHREX, INC. K040907 07/01/2004
arthrex retrobutton, 15mm, 60mm, retrobutton, long, 15mm, 60mm ARTHREX, INC. K062747 09/29/2006
arthrex puddu osteotomy system ARTHREX, INC. K973812 06/10/1998
arthrex plates, screws, and staples Arthrex, Inc. K150456 04/29/2015
arthrex minimally invasive ankle fusion plate Arthrex, Inc. K190953 10/16/2019
arthrex mesh plate system Arthrex, Inc. K170547 09/01/2017
-
-