Last synced on 2 May 2025 at 11:05 pm

Navigated Anterolateral Disc Prep Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211441
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2021
Days to Decision
30 days
Submission Type
Summary

Navigated Anterolateral Disc Prep Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211441
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2021
Days to Decision
30 days
Submission Type
Summary