Last synced on 19 July 2024 at 11:05 pm

Bonafix TiBase

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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