Identity
- Trade Name
- Medtronic Resuable Instruments FDA UDI
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
- Device Name
- POPPER 7971001 SMALL FDA UDI
- Model / Reference
- 7971001 FDA UDI
- Description
- POPPER 7971001 SMALL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00613994309266 FDA UDI
- 510(k) Number
- K071033 FDA UDI
- FDA Product Code
- MQP FDA UDI
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 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
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic prosthesis implantation positioning instrument, reusable
Medtronic Resuable Instruments by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K071033 also covers:
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- T2™ Spinal 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 b4297e15-4def-4445-a87f-439483485fbb 35 fields · synced May 29, 2026