NEUROMOD STIMULATOR MODEL 3723— 510(k) K780186
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K780186 for NEUROMOD STIMULATOR MODEL 3723, Substantially Equivalent on 1978-03-02. Applicant: Medtronic Vascular.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.