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CAVUX™ Cervical Cage-L 6x12x15mm 7 deg

FDA UDI

Class II (US FDA UDI)

by Providence Medical Technology, Inc.

Identity

Trade Name
CAVUX™ Cervical Cage-L 6x12x15mm 7 deg FDA UDI
Generic Name
Implantable cervical facet joint distractor FDA UDI
Device Name
CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. FDA UDI
Model / Reference
PD-31-600 FDA UDI
Description
CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. FDA UDI

Identifiers

Catalog Number
PD-31-600 FDA UDI
Primary DI / UDI-DI
00852776006256 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Implantable cervical facet joint distractor 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
Sterilization Method
Radiation Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Implantable cervical facet joint distractor

CAVUX™ Cervical Cage-L 6x12x15mm 7 deg by Providence Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable cervical facet joint distractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Providence Medical Technology, Inc.

Sources (1)

  • FDA UDI 85d6d943-563c-474b-a721-a69e06be8c09 34 fields · synced May 30, 2026