Last synced on 14 November 2025 at 11:06 pm

Bonafix TiBase

Page Type
Cleared 510(K)
510(k) Number
K221673
510(k) Type
Traditional
Applicant
Zentek Medical LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2023
Days to Decision
400 days
Submission Type
Summary

Bonafix TiBase

Page Type
Cleared 510(K)
510(k) Number
K221673
510(k) Type
Traditional
Applicant
Zentek Medical LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2023
Days to Decision
400 days
Submission Type
Summary