Last synced on 14 November 2025 at 11:06 pm

AVAmax Vertebral Balloon, AVAflex Vertebral Balloon

Page Type
Cleared 510(K)
510(k) Number
K162062
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2016
Days to Decision
98 days
Submission Type
Summary

AVAmax Vertebral Balloon, AVAflex Vertebral Balloon

Page Type
Cleared 510(K)
510(k) Number
K162062
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2016
Days to Decision
98 days
Submission Type
Summary