Identity
- Trade Name
- V-STRUT Vertebral Implant FDA UDI
- Generic Name
- Vertebral body prosthesis FDA UDI
- Device Name
- V-STRUT© Vertebral Implant 4.5-L55 FDA UDI
- Model / Reference
- 34555 FDA UDI
- Description
- V-STRUT© Vertebral Implant 4.5-L55 FDA UDI
Identifiers
- Catalog Number
- 34555 FDA UDI
- Primary DI / UDI-DI
- 03770007907820 FDA UDI
- FDA Product Code
- NDN FDA UDILOD FDA UDI
- GMDN Term
- Vertebral body prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3027 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
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 4.5 Millimeter FDA UDILength — 55 Millimeter FDA UDI
Category: Vertebral body prosthesis
V-STRUT Vertebral Implant by Hyprevention Sas — 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
- Hyprevention Sas
Sources (1)
- FDA UDI d8cf9e97-56a0-4ab5-aa96-62b811b0dce5 35 fields · synced May 30, 2026