• 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
-
81 to 90 of 117 Results
ProductCode: HRS Applicant: SYNTHES (USA) Decision Date To: 04/25/2024
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
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]
synthes 4.5 mm lcp posterolateral proximal femur plates SYNTHES (USA) K070208 03/28/2007
synthes 4.5 mm lcp straight reconstruction plates SYNTHES (USA) K051986 09/08/2005
synthes 4.5 mm titanium lcp proximal tibia plating system SYNTHES (USA) K023802 01/28/2003
synthes 4.5 mm va-lcp curved condylar system SYNTHES (USA) K083025 01/14/2009
synthes anatomical locking plate system SYNTHES (USA) K961413 08/07/1996
synthes ankle arthrodesis plate SYNTHES (USA) K013415 01/11/2002
synthes calcaneal plate SYNTHES (USA) K020401 05/08/2002
synthes curved reconstruction plate SYNTHES (USA) K011334 07/27/2001
synthes dorsal distal radius plate (ddrp) system SYNTHES (USA) K962616 09/03/1996
synthes high tibial osteotomy (hto) system SYNTHES (USA) K962894 12/17/1996
-
-