Last synced on 3 April 2026 at 11:13 pm

Atlas Spine Project X Expandable Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251969
510(k) Type
Traditional
Applicant
Atlas Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2025
Days to Decision
50 days
Submission Type
Statement

Atlas Spine Project X Expandable Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251969
510(k) Type
Traditional
Applicant
Atlas Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2025
Days to Decision
50 days
Submission Type
Statement