• 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 6 of 6 Results
ProductCode: NKB Applicant: GENESYS SPINE Decision Date To: 05/07/2024
Results per Page
New Search  
Export all 6 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]
tilock modular spinal system Genesys Spine K172469 11/30/2017
tilock2 spinal system Genesys Spine K171838 07/19/2017
genesys spine tilock cortical spinal system Genesys Spine K161914 08/09/2016
genesys spine tilock2 spinal system Genesys Spine K152039 10/28/2015
genesys spine tilock system GENESYS SPINE K103671 07/21/2011
tilock pedicle screw system GENESYS SPINE K100757 07/01/2010
-
-