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AVAMAX VERTEBRAL BALLOON SYSTEM, 8G, AVAMAX VERTEBRAL BALLOON SYSTEM, 10G, AVAMAX VERTEBRAL BALLOON SYSTEM, 11G

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131820
510(k) Type
Traditional
Applicant
Care Fusion
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2013
Days to Decision
106 days
Submission Type
Summary

AVAMAX VERTEBRAL BALLOON SYSTEM, 8G, AVAMAX VERTEBRAL BALLOON SYSTEM, 10G, AVAMAX VERTEBRAL BALLOON SYSTEM, 11G

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131820
510(k) Type
Traditional
Applicant
Care Fusion
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2013
Days to Decision
106 days
Submission Type
Summary