Identity
- Trade Name
- CD HORIZON® Spinal System FDA UDI
- Generic Name
- Metal-polymer composite spinal interbody fusion cage FDA UDI
- Device Name
- SPACER XIB1102-009 18MM VSTCK 12 DEG FDA UDI
- Model / Reference
- XIB1102-009 FDA UDI
- Description
- SPACER XIB1102-009 18MM VSTCK 12 DEG FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00721902666971 FDA UDI
- 510(k) Number
- K021791 FDA UDI
- FDA Product Code
- MQP FDA UDI
- GMDN Term
- Metal-polymer composite spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Metal-polymer composite spinal interbody fusion cage
CD HORIZON® Spinal System by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metal-polymer composite spinal interbody fusion cage.
- Battalion Universal Spinal Spacer System — ALPHATEC SPINE, INC. · Class II
- Irix-A Lumbar Integrated Fusion System — Xtant Medical Holdings, Inc. · Class II
- Tyber Medical — Tyber Medical · Class II
- Reef TA — SeaSpine Orthopedics Corporation · Class II
- 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
Cleared under the same submission
K021791 also covers:
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
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
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI 4e9413e3-f3cc-40fd-bf0f-8a1530e9e8a4 36 fields · synced Jun 1, 2026