Identity
- Trade Name
- Katalyst™ Bipolar Radial Head System FDA UDI
- Generic Name
- Elbow radius prosthesis FDA UDI
- Device Name
- The Katalyst Radial Stem restores the support and bearing surfaces of the radial head in the face of fracture, arthritis or failed prior implantation. FDA UDI
- Model / Reference
- 221685 FDA UDI
- Description
- The Katalyst Radial Stem restores the support and bearing surfaces of the radial head in the face of fracture, arthritis or failed prior implantation. FDA UDI
Identifiers
- Catalog Number
- 221685 FDA UDI
- Primary DI / UDI-DI
- 10381780065876 FDA UDI
- FDA Product Code
- KWI FDA UDI
- GMDN Term
- Elbow radius prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3170 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
Yes
FDA UDI
Katalyst™ Bipolar Radial Head System by Integra Lifesciences Corp. — 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
- Integra Lifesciences Corp.
Sources (1)
- FDA UDI 228998dd-50f1-449a-bc61-921459b04da4 38 fields · synced May 30, 2026