Identity
- Trade Name
- Fortress Pedicular Fixation FDA UDI
- Generic Name
- Instrument table FDA UDI
- Device Name
- Case 2 Base FDA UDI
- Model / Reference
- 64-12-02 FDA UDI
- Description
- Case 2 Base FDA UDI
Identifiers
- Catalog Number
- 646-0002 FDA UDI
- Primary DI / UDI-DI
- M7406460002 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Instrument table FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- 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
MR Unsafe FDA UDI
Category: Instrument table
Fortress Pedicular Fixation by Spineology Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Spineology Inc.
Sources (1)
- FDA UDI 6db1d1e8-2ec8-4e66-8d11-e8100ef4c401 35 fields · synced May 30, 2026