Last synced on 25 January 2026 at 3:41 am

AXXION LIGHT GUIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082992
510(k) Type
Traditional
Applicant
Spinal Elements, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/2009
Days to Decision
134 days
Submission Type
Summary

AXXION LIGHT GUIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082992
510(k) Type
Traditional
Applicant
Spinal Elements, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/2009
Days to Decision
134 days
Submission Type
Summary