• 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 7 of 7 Results
ProductCode: OVD Applicant: BIOMET SPINE Decision Date To: 05/16/2024
Results per Page
New Search  
Export all 7 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]
avenue p cage system Zimmer Biomet Spine, Inc. K181096 01/15/2019
biomet fusion system Zimmer Biomet Spine Inc. K163543 02/28/2017
biomet fusion system BIOMET SPINE K141791 10/09/2014
solitarie peek anterior spinal system-to be called colitaire 35 BIOMET SPINE & BONE HEALING TECHNOLOGIES K120557 03/19/2012
solitaire and solitaire peek anterior spinal system BIOMET SPINE K093629 03/09/2010
solitaire anterior spinal system BIOMET SPINE K081501 07/02/2008
solitaire peek-optima anterior spinal system BIOMET SPINE K081395 06/25/2008
-
-