Last synced on 14 November 2025 at 11:06 pm

AVAFLEX VERTEBRAL BALLOON SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131824
510(k) Type
Traditional
Applicant
CAREFUSION
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)
510(k) Number
K131824
510(k) Type
Traditional
Applicant
CAREFUSION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2013
Days to Decision
105 days
Submission Type
Summary