RESTORE, RESTOREPRIME, RESTOREADVANCED, RESTORE PRIME ADVANCED, AND RESTOREULTRA NEUROSTIMULATION SYSTEMS
FDA premarket approval P840001/S122 · decided 2008-12-08
Approval details
- PMA number
- P840001
- Supplement
- S122
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- RESTORE, RESTOREPRIME, RESTOREADVANCED, RESTORE PRIME ADVANCED, AND RESTOREULTRA NEUROSTIMULATION SYSTEMS
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- Medtronic Neuromodulation
- Date received
- 2008-10-08
- Decision date
- 2008-12-08
- Days to decision
- 61 days
- Decision code
- APPR
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- APPROVAL FOR THE ADDITION OF A STABILIZING COIL TO THE MODEL 37083 EXTENSION, A ¿POST-CURE¿ PROCESSING STEP AT THE DISTAL END OF THE MODELS 37083 AND 37082 EXTENSIONS, AND A PROXIMAL BOND STRENGTH (THERMAL BOND) DESIGN REQUIREMENT FOR MODELS 37083 AND 37082 EXTENSIONS.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |