Identity
- Trade Name
- neoWave C FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- CERVICAL TRIAL, FLAT 19X14, 6MM 0° NT FDA UDI
- Model / Reference
- 20-TFN-9406 FDA UDI
- Description
- CERVICAL TRIAL, FLAT 19X14, 6MM 0° NT FDA UDI
Identifiers
- Catalog Number
- N/A FDA UDI
- Primary DI / UDI-DI
- 00818345025004 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Spinal implant trial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
neoWave C by Xenix Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Spinal implant trial.
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- IdentiTi — ALPHATEC SPINE, INC. · Class II
- MLX — Nuvasive, Inc. · Class I
- IdentiTi — ALPHATEC SPINE, INC. · Class II
- ROI-A — Ldr Spine USA · Class II
Cleared under the same submission
K180401 also covers:
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
- TiWAVE C Cervical Cage System — Kalitec Direct LLC
K222988 also covers:
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
- Ti3D CERVICAL — Xenix Medical
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Xenix Medical
Sources (1)
- FDA UDI 76346880-488b-45cf-afc8-5983ceb5da6a 36 fields · synced May 31, 2026