Last synced on 12 July 2024 at 11:04 pm

SureTune4 Software

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN210003
510(k) Type
Direct
Applicant
Medtronic Neuromodulation
Country
United States
FDA Decision
Deleted
Decision Date
8/23/2021
Days to Decision
201 days

SureTune4 Software

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN210003
510(k) Type
Direct
Applicant
Medtronic Neuromodulation
Country
United States
FDA Decision
Deleted
Decision Date
8/23/2021
Days to Decision
201 days