Identity
- Trade Name
- FortiCore® FDA UDI
- Generic Name
- Metal-polymer composite spinal interbody fusion cage FDA UDI
- Device Name
- FortiCore® Cervical Spacer 11x16x14, (6°) FDA UDI
- Model / Reference
- 11204-1611 FDA UDI
- Description
- FortiCore® Cervical Spacer 11x16x14, (6°) FDA UDI
Identifiers
- Catalog Number
- 11204-1611 FDA UDI
- Primary DI / UDI-DI
- 00814216020765 FDA UDI
- FDA Product Code
- ODP FDA UDI
- GMDN Term
- Metal-polymer composite spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 16 Millimeter FDA UDIWidth — 14 Millimeter FDA UDIHeight — 11 Millimeter FDA UDI
Category: Metal-polymer composite spinal interbody fusion cage
FortiCore® by Nanovis Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metal-polymer composite spinal interbody fusion cage.
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- ROI-C — Ldr Spine USA · Class II
- LUCENT XP ARC — SPINAL ELEMENTS, INC. · Class II
- Shoreline ACS — SeaSpine Orthopedics Corporation · Class II
- MIDLINE II-Ti — Centinel Spine, LLC · Class II
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
- Nanovis Spine, Llc
Sources (1)
- FDA UDI 656f3527-d8a4-4602-95d0-106e49a83c73 36 fields · synced Jun 8, 2026