• 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 39 Results
ProductCode: KTT Applicant: SYNTHES (USA) Decision Date To: 04/23/2024
 
 1 
 2 
 3 
 4 
 > 
Results per Page
New Search  
Export all 39 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]
3.5 mm lcp distal humerus system SYNTHES (USA) K033995 03/01/2004
adjustable large fixator system SYNTHES (USA) K010344 05/03/2001
dynamic hip screw SYNTHES (USA) K791619 08/28/1979
small fragment dynamic compression locking (dcl) system SYNTHES (USA) K000684 04/28/2000
synthes (usa) articulating distal radius (adrf) system SYNTHES (USA) K984498 02/18/1999
synthes (usa) ddhs/dcs system modification SYNTHES (USA) K964259 01/09/1997
synthes (usa) distraction osteogenesis system SYNTHES (USA) K051600 07/27/2005
synthes (usa) external fixation component line extension - mr safe SYNTHES (USA) K043039 01/18/2005
synthes (usa) large fragment locking compression plate (lcp) system-t plate SYNTHES (USA) K010766 06/12/2001
synthes (usa) lcp curved plates SYNTHES (USA) K041911 09/08/2004
-
-