Identity
- Trade Name
- KEYSTONE FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- KEYSTONE GRAFT DELIVERY INSTRUMENTS FIBULAR TRIAL PARALLEL 12mm FDA UDI
- Model / Reference
- 282112112 FDA UDI
- Description
- KEYSTONE GRAFT DELIVERY INSTRUMENTS FIBULAR TRIAL PARALLEL 12mm FDA UDI
Identifiers
- Catalog Number
- 282112112 FDA UDI
- Primary DI / UDI-DI
- 10705034204734 FDA UDI
- FDA Product Code
- HWT FDA UDI
- GMDN Term
- Spinal implant trial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4800 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Keystone by Depuy Spine, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Depuy Spine, Inc.
Sources (1)
- FDA UDI 0ee6c841-db3a-4f6b-a43d-b7de538f8a4c 36 fields · synced May 31, 2026