Identity
- Trade Name
- RBK Patello Femoral FDA UDI
- Generic Name
- Uncoated knee femur prosthesis, metallic FDA UDI
- Device Name
- RBK Patello Femoral Size 1 Left FDA UDI
- Model / Reference
- GO-6000-1PFL-01 FDA UDI
- Description
- RBK Patello Femoral Size 1 Left FDA UDI
Identifiers
- Catalog Number
- GO-6000-1PFL-01 FDA UDI
- Primary DI / UDI-DI
- 09340499017754 FDA UDI
- 510(k) Number
- K050473 FDA UDI
- FDA Product Code
- KRR FDA UDI
- GMDN Term
- Uncoated knee femur prosthesis, metallic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3540 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
RBK Patello Femoral by Global Manufacturing Technology Pty Limited — 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
- Global Manufacturing Technology Pty Limited
Sources (1)
- FDA UDI 0436bc0d-7124-4717-879d-0f3602dd40fb 38 fields · synced May 29, 2026