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VK100 Percutaneous Vertebral Augmentation System

Page Type
Cleared 510(K)
510(k) Number
K192403
510(k) Type
Traditional
Applicant
BONWRx Ltd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2019
Days to Decision
66 days
Submission Type
Summary

VK100 Percutaneous Vertebral Augmentation System

Page Type
Cleared 510(K)
510(k) Number
K192403
510(k) Type
Traditional
Applicant
BONWRx Ltd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2019
Days to Decision
66 days
Submission Type
Summary