Identity
- Trade Name
- CAVUX Cervical Cage-T FDA UDI
- Generic Name
- Metallic spinal interbody fusion cage FDA UDI
- Device Name
- The CAVUX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. FDA UDI
- Model / Reference
- PD-31-100 FDA UDI
- Description
- The CAVUX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. FDA UDI
Identifiers
- Catalog Number
- PD-31-100 FDA UDI
- Primary DI / UDI-DI
- 00852776006010 FDA UDI
- 510(k) Number
- K122801 FDA UDI
- FDA Product Code
- ODP FDA UDI
- GMDN Term
- Metallic spinal interbody fusion cage 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
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
Yes
FDA UDI
Radiation Sterilization FDA UDI
Category: Metallic spinal interbody fusion cage
CAVUX Cervical Cage-T by Providence Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metallic spinal interbody fusion cage.
- KODIAK CERVICAL IMPLANT, 14x16mm, 10mmx6° — MET 1 TECHNOLOGIES, LLC · Class II
- Peridot-PT Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
- CoRoent — Nuvasive, Inc. · Class II
- Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II
- MectaLIF 3D — Medacta International · Class II
- PILLAR TL — Orthofix US LLC · Class II
- Solar™ Interbody Fusion System — Degen Medical · Class II
- Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
Cleared under the same submission
K122801 also covers:
- CAVUX CERVICAL CAGE-X, 5MM — PROVIDENCE MEDICAL TECHNOLOGY, INC.
- CAVUX Cage-LX, 4mm — PROVIDENCE MEDICAL TECHNOLOGY, INC.
- CAVUX Cervical Cage-B — PROVIDENCE MEDICAL TECHNOLOGY, INC.
- CAVUX Cervical Cage-X — PROVIDENCE MEDICAL TECHNOLOGY, INC.
- CAVUX™ Cervical Cage SB — PROVIDENCE MEDICAL TECHNOLOGY, INC.
- CAVUX™ Cervical Cage-B 5mm — PROVIDENCE MEDICAL TECHNOLOGY, INC.
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
- Providence Medical Technology, Inc.
Sources (1)
- FDA UDI 91864f13-7168-4db4-a8b2-5ec314ee9a09 35 fields · synced May 30, 2026