Identity
- Trade Name
- SCP® PF Knee Kit FDA UDI
- Generic Name
- Bone graft delivery kit FDA UDI
- Model / Reference
- 464503 FDA UDI
Identifiers
- Catalog Number
- 464503 FDA UDI
- Primary DI / UDI-DI
- 00889024501294 FDA UDI
- FDA Product Code
- OJH FDA UDI
- GMDN Term
- Bone graft delivery kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bone graft delivery kit
SCP® PF Knee Kit by Zimmer Knee Creations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone graft delivery kit.
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Fusion Biologics — FUSION ORTHOPEDICS, LLC · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Fusion Biologics — FUSION ORTHOPEDICS, LLC · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Zimmer Knee Creations, Inc.
Sources (1)
- FDA UDI d30c9461-c8dc-47bf-8cf7-7503544cc8f2 35 fields · synced Jun 9, 2026