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TRANS1 AXIALIF PLUS

Page Type
Cleared 510(K)
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)
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