Identity
- Trade Name
- ACCURIAN™ FDA UDI
- Generic Name
- Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI
- Device Name
- INTRODUCER AI0004 50MM 12MM ENHANCED FDA UDI
- Model / Reference
- AI0004 FDA UDI
- Description
- INTRODUCER AI0004 50MM 12MM ENHANCED FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20763000312248 FDA UDI
- 510(k) Number
- K181864 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Dimensions & Sizes
- Size
- Needle Gauge — 17.0 Gauge FDA UDILength — 50.0 Millimeter FDA UDI
Category: Percutaneous radio-frequency ablation probe cannula, single-use
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 cannula, single-use.
- OWL — Diros Technology, Inc. · Class II
- OWL — Diros Technology, Inc. · Class II
- RadiOpaque Radiofrequency Cannula — Avanos Medical, Inc. · Class II
- OWL — Diros Technology, Inc. · Class II
- Halyard — Avanos Medical, Inc. · Class II
- RadiOpaque Radiofrequency Cannula — Avanos Medical, Inc. · Class II
- LCCS — Lccs Products Limited · Class II
- OWL — Diros Technology, Inc. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI 3cbd28ee-8935-46ee-92f2-7272d80a98ea 37 fields · synced May 30, 2026