Senza ACCK4320
Senza ACCK4320 is a Class III device made by Nevro Corporation, approved under FDA PMA P130022 on 8 May 2015 and listed in FDA GUDID since 24 Mar 2021 (UDI-DI 00813426020688), active as of 22 Oct 2026.
Active
PMA
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00813426020688 | Date24 Mar 2021 | StatusListed |
| United States | FDA PMAAPPR | NumberP130022 | Date8 May 2015 | StatusActive |
Official records
- AccessGUDID record 00813426020688
- FDA PMA database P130022
Across registries
- FDA PMA P130022 decided 8 May 2015 Active
- FDA GUDID UDI-DI 00813426020688 listed 24 Mar 2021 Listed
Timeline
- Approved FDA PMA P130022
- Listed FDA GUDID 00813426020688
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Trade name
- Senza
- Generic name
- Active implantable device control magnet
- Model / Ref / Catalog
- ACCK4320
- Primary DI / UDI-DI
- 00813426020688
- PMA number
- FDA product code
- LGW
- GMDN term
- Active implantable device control magnet
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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