Last synced on 25 January 2026 at 3:41 am

TRANS1 AXIALIF PLUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102334
510(k) Type
Traditional
Applicant
Trans1 Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2011
Days to Decision
209 days
Submission Type
Summary

TRANS1 AXIALIF PLUS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102334
510(k) Type
Traditional
Applicant
Trans1 Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2011
Days to Decision
209 days
Submission Type
Summary