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 8 of 8 Results
ProductCode: MAX Applicant: GENESYS SPINE Decision Date To: 09/19/2024
Results per Page
New Search  
Export all 8 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]
genesys spine 3dp lumbar interbody system Genesys Spine K220096 03/09/2022
genesys spine 3dp lumbar interbody system Genesys Spine K182987 12/12/2019
genesys spine apache interbody fusion system Genesys Spine K171656 07/13/2017
genesys spine apache® anterior lumbar interbody fusion system GENESYS SPINE K161438 11/08/2016
genesys spine apache® lateral lumbar interbody fusion system Genesys Spine K161404 07/21/2016
genesys spine apache interbody fusion system GENESYS SPINE K153123 04/26/2016
genesys spine apache lateral lumbar interbody fusion system GENESYS SPINE K130913 12/13/2013
genesys spine interbody fusion system GENESYS SPINE K103034 12/10/2010
-
-