Identity
- Trade Name
- OsteoCool™ 2.0 RF Ablation System FDA UDI
- Generic Name
- Percutaneous radio-frequency ablation system generator FDA UDI
- Device Name
- HUB OC04-100 OC 2.0 100W FDA UDI
- Model / Reference
- OC04-100 FDA UDI
- Description
- HUB OC04-100 OC 2.0 100W FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000764043 FDA UDI
- 510(k) Number
- K233830 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Percutaneous radio-frequency ablation system generator 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
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
Category: Percutaneous radio-frequency ablation system generator
OsteoCool™ 2.0 RF Ablation System by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Percutaneous radio-frequency ablation system generator.
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Cleared under the same submission
K233830 also covers:
- OsteoCool™ 2.0 RF Ablation System — MEDTRONIC SOFAMOR DANEK, INC.
- OsteoCool™ 2.0 RF Ablation System — MEDTRONIC SOFAMOR DANEK, INC.
- OsteoCool™ 2.0 RF Ablation System — MEDTRONIC SOFAMOR DANEK, INC.
- OsteoCool™ 2.0 RF Ablation System — MEDTRONIC SOFAMOR DANEK, INC.
- OsteoCool™ 2.0 RF Ablation System — MEDTRONIC SOFAMOR DANEK, INC.
- OsteoCool™ 2.0 RF Ablation System — 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 cacd2d2b-f05a-4ec5-b59f-f2ad6f20eca2 36 fields · synced May 29, 2026