Identity
- Trade Name
- VERTICALE FDA UDI
- Generic Name
- Spinal bone screw, non-bioabsorbable FDA UDI
- Device Name
- VERTICALE Poly Screw ST 7.2x70mm,can+fen FDA UDI
- Model / Reference
- S-VPS-7270-KF2 FDA UDI
- Description
- VERTICALE Poly Screw ST 7.2x70mm,can+fen FDA UDI
Identifiers
- Catalog Number
- S-VPS-7270-KF2 FDA UDI
- Primary DI / UDI-DI
- 04054896039251 FDA UDI
- FDA Product Code
- KWP FDA UDINKB FDA UDI
- GMDN Term
- Spinal bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3050 FDA UDI888.3070 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 — 70 Millimeter FDA UDIOuter Diameter — 7.2 Millimeter FDA UDI
Category: Spinal bone screw, non-bioabsorbable
Verticale by Silony Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal bone screw, non-bioabsorbable.
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- AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
- Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · 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
- Silony Medical GmbH
Sources (1)
- FDA UDI d741d239-8582-4b42-bb33-3a2e565a93f6 35 fields · synced May 31, 2026