Identity
- Trade Name
- MaxFuse VBR, 10 (D) x 12 (W) x 26 (H) FDA UDI
- Generic Name
- Vertebral body prosthesis FDA UDI
- Device Name
- 10 (D) x 12 (W) x 26 (H) FDA UDI
- Model / Reference
- 62-1012-41 FDA UDI
- Description
- 10 (D) x 12 (W) x 26 (H) FDA UDI
Identifiers
- Catalog Number
- 62-1012-41 FDA UDI
- Primary DI / UDI-DI
- 00846468055073 FDA UDI
- FDA Product Code
- MQP FDA UDI
- GMDN Term
- Vertebral body prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MaxFuse VBR, 10 (D) x 12 (W) x 26 (H) by Pioneer Surgical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Pioneer Surgical Technology, Inc.
Sources (1)
- FDA UDI 6263ae87-96b9-4de4-bc4c-0ccfd287c05c 36 fields · synced Jun 1, 2026