← Back to catalogue
Altius® Direct Electrical Nerve Stimulation System
FDA PMAClass III (US FDA PMA)
PMA P230020
Identity
- Trade Name
- Altius® Direct Electrical Nerve Stimulation System FDA PMA
- Generic Name
- stimulator, nerve terminus, totally implanted for chronic intractable post-amputation pain of the lower limb FDA PMA
Identifiers
- PMA Number
- P230020 FDA PMA
- FDA Product Code
- SAZ FDA PMA
Classification
- Device Class
- Class III FDA PMA
- Advisory Committee
- Neurology FDA PMA
- FDA Decision
- APPR Approved FDA PMA
Altius® Direct Electrical Nerve Stimulation System by Neuros Medical, Inc. — Class III — FDA_PMA — listed in FDA PMA — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_PMA
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA PMA | United States | FDA_PMA | P230020 | Class III | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Neuros Medical, Inc.
Sources (1)
- FDA PMA P230020 23 fields · synced Jun 18, 2026