← Back to catalogue
Femur And Tibia Cutting Block Adapter
FDA UDIClass II (US FDA UDI)
by Brainlab SE
Identity
- Trade Name
- Femur And Tibia Cutting Block Adapter FDA UDI
- Generic Name
- Robotic surgical navigation system FDA UDI
- Model / Reference
- 52568C FDA UDI
Identifiers
- Catalog Number
- 52568C FDA UDI
- Primary DI / UDI-DI
- 04056481002190 FDA UDI
- 510(k) Number
- K102990 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Robotic surgical navigation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Femur And Tibia Cutting Block Adapter by Brainlab SE — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K102990 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Brainlab SE
Sources (1)
- FDA UDI 1efb823b-83f1-4ee2-a5ec-9c921cb4d8c2 36 fields · synced May 31, 2026