Last synced on 12 October 2025 at 8:21 pm

OneLIF™ Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251459
510(k) Type
Special
Applicant
NovApproach Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2025
Days to Decision
31 days
Submission Type
Summary

OneLIF™ Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251459
510(k) Type
Special
Applicant
NovApproach Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2025
Days to Decision
31 days
Submission Type
Summary