Identity
- Trade Name
- POWEREASE™ Instruments FDA UDI
- Generic Name
- Orthopaedic implantable-device cutter FDA UDI
- Device Name
- COUNTER TORQUE 2346011 4.75 MAS/FAS FDA UDI
- Model / Reference
- 2346011 FDA UDI
- Description
- COUNTER TORQUE 2346011 4.75 MAS/FAS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00613994917683 FDA UDI
- 510(k) Number
- K111520 FDA UDI
- FDA Product Code
- HWE FDA UDIHBE FDA UDIGWF FDA UDI
- GMDN Term
- Orthopaedic implantable-device cutter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI882.4310 FDA UDI882.1870 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic implantable-device cutter
POWEREASE™ Instruments by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K111520 also covers:
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- POWEREASE™ Instruments — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI f81a45bb-0f50-4b51-9b2c-ea740f0f75b3 35 fields · synced Jun 8, 2026