Identity
- Trade Name
- Nevro® FDA UDI
- Generic Name
- Implantable pulse generator port plug FDA UDI
- Device Name
- IPG Port Plug Kit FDA UDI
- Model / Reference
- ACCK7000 FDA UDI
- Description
- IPG Port Plug Kit FDA UDI
Identifiers
- Catalog Number
- ACCK7000 FDA UDI
- Primary DI / UDI-DI
- 00813426020275 FDA UDI
- PMA Number
- P130022 FDA UDI
- FDA Product Code
- LGW FDA UDI
- GMDN Term
- Implantable pulse generator port plug FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Category: Implantable pulse generator port plug
Nevro® by Nevro Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Implantable pulse generator port plug.
- BIOTRONIK — BIOTRONIK SE & Co. KG · Class III
- Precision Spectra ™ — Boston Scientific Neuromodulation · Class III
- VV-PLUG — Oscor Inc. · Class III
- SJM™ — ST. JUDE MEDICAL, INC. · Class III
- IS4/DF4 PLUG — Oscor Inc. · Class II
- Eon™ — ST. JUDE MEDICAL, INC. · Class III
- Eon™ — ST. JUDE MEDICAL, INC. · Class III
- VV-Plug — Oscor Inc. · Class II
Cleared under the same submission
P130022 also covers:
- Nevro — Nevro Corporation
- Nevro — Nevro Corporation
- Nevro — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
- Nevro® — Nevro Corporation
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nevro Corporation
Sources (1)
- FDA UDI 72aa5062-8045-4e87-a81d-cb43d1044cec 36 fields · synced Jun 8, 2026