- Physicians Office Resource

Flexible Extensions
Aliquot - 2110-0507

Device Description

A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.

Environmental Conditions

Storage Environment Temperature - Degrees Celsius

30.00
20.00

Device Sizes

Total Volume: 5.0 Cubic Centimeter

Total Volume: 5.0 Cubic Centimeter

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

Code: KIH

Device Name: Dispenser, Cement

Device Class: 1

Physical State: N/A

Definition: N/A

Submission Type ID: 4

Review Panel: OR

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: N/A

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: N

Target Area: N/A

Regulation Number: 888.4200

Third Party Flag: N

Medical Specialty: OR

Device Identifiers

Device Id: 30808232001137

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

Device Id: 00808232001136

Device Type: Unit of Use

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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