Identity
- Trade Name
- Ventura NanoMetalene System FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- Ventura NM Trial, 9mm x 20mm x 10mm, Lordotic FDA UDI
- Model / Reference
- 93-3705 FDA UDI
- Description
- Ventura NM Trial, 9mm x 20mm x 10mm, Lordotic FDA UDI
Identifiers
- Catalog Number
- 93-3705 FDA UDI
- Primary DI / UDI-DI
- 10889981150815 FDA UDI
- 510(k) Number
- K173022 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Spinal implant trial 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Spinal implant trial
Ventura NanoMetalene System by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K173022 also covers:
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
- Ventura NanoMetalene System — SeaSpine Orthopedics Corporation
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
- SeaSpine Orthopedics Corporation
Sources (1)
- FDA UDI 8c5efc7b-a6bc-467c-9324-853797b592ea 37 fields · synced Jun 8, 2026