Identity
- Trade Name
- SpaceVision® PLIF FDA UDI
- Generic Name
- Polymeric spinal fusion cage, sterile FDA UDI
- Device Name
- Sterile PLIF cage H11-L29-A04 FDA UDI
- Model / Reference
- SPL1-C11-29-04 FDA UDI
- Description
- Sterile PLIF cage H11-L29-A04 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03663136029269 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Polymeric spinal fusion cage, sterile 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
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
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
- Angle — 04 degree FDA UDILength — 29 Millimeter FDA UDIHeight — 11 Millimeter FDA UDI
Category: Polymeric spinal fusion cage, sterile
SpaceVision® PLIF by Spine Vision, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Spine Vision, Inc.
Sources (1)
- FDA UDI eb15b5c3-9ce6-4e76-8955-2d2fe56d047a 35 fields · synced Jun 8, 2026