- Physicians Office Resource

Cement Cannula
VertePort - 0306310000

Device Description

A sterile, manual, tubular device designed to create a percutaneous access channel into a vertebral body prior to and during injection of orthopaedic cement into the vertebral body during kyphoplasty. It is typically inserted under fluoroscopic guidance to treat a patient diagnosed with vertebral compression fractures (VCFs) in the lumbar or thoracic region of the spine. The device is typically made of stainless steel with an attached plastic handle and available in a kit of several equal size cannulae (e.g., 3 or 6) to provide access to one or more sites of intervention. This is a single-use device.

Environmental Conditions

No Data Available

Device Sizes

Needle Gauge: 8.0 Gauge

Needle Gauge: 8.0 Gauge

Device Sterilization

Device Sterile: True

Sterilization Prior To Use: False

Sterilization Methods: No Data Available

Product Codes

Code: OAR

Device Name: Injector, Vertebroplasty (Does Not Contain Cement)

Device Class: 1

Physical State: plastic syringe type device -- some embodiments may include levers or screws to increase injection force or control

Definition: Intended for injection of vertebroplasty bone cement for the fixation of pathological fractures of the vertebral body using vertebroplasty or kyphoplasty procedures. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancers, myeloma).

Submission Type ID: 4

Review Panel: OR

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: Uses mechanical force to inject bone cement into vertebra

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: N

Target Area: vertebra

Regulation Number: 888.4200

Third Party Flag: N

Medical Specialty: OR

Device Identifiers

Device Id: 37613252183373

Device Type: Package

DeviceId Issuing Agency: GS1

Contains DI Number: 07613252183372

Package Quantity: 18

Package Discontinue Date: N/A

Package Status: In Commercial Distribution

Package Type: pack

Device Id: 07613252183372

Device Type: Primary

DeviceId Issuing Agency: GS1

Contains DI Number: N/A

Package Quantity: N/A

Package Discontinue Date: N/A

Package Status: N/A

Package Type: N/A

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