Last synced on 14 November 2025 at 11:06 pm

Ziehm RFD 3D Tracker

Page Type
Cleared 510(K)
510(k) Number
K180816
510(k) Type
Traditional
Applicant
Medtronic Navigation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2018
Days to Decision
104 days
Submission Type
Summary

Ziehm RFD 3D Tracker

Page Type
Cleared 510(K)
510(k) Number
K180816
510(k) Type
Traditional
Applicant
Medtronic Navigation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2018
Days to Decision
104 days
Submission Type
Summary