Last synced on 25 January 2026 at 3:41 am

Annex® 2 Adjacent Level System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251131
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2025
Days to Decision
56 days
Submission Type
Summary

Annex® 2 Adjacent Level System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251131
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2025
Days to Decision
56 days
Submission Type
Summary