• 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 117 Results
ProductCode: HRS Applicant: SYNTHES (USA) Decision Date To: 04/25/2024
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
Results per Page
New Search  
Export all 117 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]
dynamic condylar screw or d.c.s. SYNTHES (USA) K840954 05/11/1984
synthes maxillofacial titanium micro set SYNTHES (USA) K912932 09/25/1991
synthes(r) titanium small reconstruction plate SYNTHES (USA) K915818 01/17/1992
synthes wire mount SYNTHES (USA) K953777 03/08/1996
volar distal radius plate SYNTHES (USA) K953644 03/08/1996
schuhli implant system SYNTHES (USA) K954963 03/22/1996
synthes anatomical locking plate system SYNTHES (USA) K961413 08/07/1996
synthes dorsal distal radius plate (ddrp) system SYNTHES (USA) K962616 09/03/1996
synthes titanium alloy volar distal radius plate (ti alloy vdrp) system SYNTHES (USA) K963798 11/27/1996
synthes high tibial osteotomy (hto) system SYNTHES (USA) K962894 12/17/1996
-
-