Identity
- Trade Name
- Accurian FDA UDI
- Generic Name
- Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar FDA UDI
- Device Name
- PROBE KIT ACCURIAN SU SS 50MM 16-22G FDA UDI
- Model / Reference
- APSD050 FDA UDI
- Description
- PROBE KIT ACCURIAN SU SS 50MM 16-22G FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20763000835631 FDA UDI
- 510(k) Number
- K181864 FDA UDI
- FDA Product Code
- GXI FDA UDI
- GMDN Term
- Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4725 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
Accurian by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar.
- ElectrodeCRF — Cambridge Interventional LLC · Class II
- BIG-TIP™ — RF Medical Co., Ltd. · Class II
- ElectrodeCRF — Cambridge Interventional LLC · Class II
- BIG-TIP™ — RF Medical Co., Ltd. · Class II
- ElectrodeCRF — Cambridge Interventional LLC · Class II
- MYOBLATE — RF Medical Co., Ltd. · Class II
- BIG-TIP™ — RF Medical Co., Ltd. · Class II
- Big-Tip — RF Medical Co., Ltd. · Class II
Cleared under the same submission
K181864 also covers:
- ACCURIAN™ — MEDTRONIC SOFAMOR DANEK, INC.
- ACCURIAN™ — MEDTRONIC SOFAMOR DANEK, INC.
- ACCURIAN™ — MEDTRONIC SOFAMOR DANEK, INC.
- ACCURIAN™ — MEDTRONIC SOFAMOR DANEK, INC.
- ACCURIAN™ — MEDTRONIC SOFAMOR DANEK, INC.
- ACCURIAN™ — MEDTRONIC SOFAMOR DANEK, INC.
- Accurian — MEDTRONIC SOFAMOR DANEK, INC.
- Accurian — MEDTRONIC SOFAMOR DANEK, INC.
- Accurian — MEDTRONIC SOFAMOR DANEK, INC.
- Accurian — MEDTRONIC SOFAMOR DANEK, INC.
- Accurian — MEDTRONIC SOFAMOR DANEK, INC.
- Accurian — MEDTRONIC SOFAMOR DANEK, INC.
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 II | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI a35fc116-22e0-4c3f-8b77-11501cc4ee87 36 fields · synced May 29, 2026