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AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092124
510(k) Type
Traditional
Applicant
Trans1 Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2010
Days to Decision
190 days
Submission Type
Summary

AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092124
510(k) Type
Traditional
Applicant
Trans1 Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2010
Days to Decision
190 days
Submission Type
Summary