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AVAFLEX VERTEBRAL BALLOON SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131824
510(k) Type
Traditional
Applicant
Care Fusion
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2013
Days to Decision
105 days
Submission Type
Summary

AVAFLEX VERTEBRAL BALLOON SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131824
510(k) Type
Traditional
Applicant
Care Fusion
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2013
Days to Decision
105 days
Submission Type
Summary