Last synced on 20 December 2024 at 11:05 pm

Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191186
510(k) Type
Traditional
Applicant
Ad-Tech Medical Instrument Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2020
Days to Decision
267 days
Submission Type
Summary

Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191186
510(k) Type
Traditional
Applicant
Ad-Tech Medical Instrument Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2020
Days to Decision
267 days
Submission Type
Summary