Last synced on 23 February 2024 at 11:04 pm

ClearPoint Bone Screw Fiducials

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233144
510(k) Type
Traditional
Applicant
ClearPoint Neuro Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
107 days
Submission Type
Summary

ClearPoint Bone Screw Fiducials

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233144
510(k) Type
Traditional
Applicant
ClearPoint Neuro Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
107 days
Submission Type
Summary