EasyManua.ls Logo

Johnson & Johnson DePuy Synthes EXPEDIUM User Manual

Johnson & Johnson DePuy Synthes EXPEDIUM
342 pages
To Next Page IconTo Next Page
To Next Page IconTo Next Page
Page #1 background imageLoading...
Page #1 background image
This document is valid only on the date printed. If unsure of the print date, please
re-print to ensure use of the latest revision of the IFU (available at www.e-ifu.com).
The onus resides with the user to ensure that the most up-to-date IFU is used.
1 of 12
0086
0902-90-067 Rev. E
en
EXPEDIUM
®
Fenestrated Screw System
Instructions for Use
IMPORTANT INFORMATION
Please Read Before Use
INDICATIONS FOR USE
The EXPEDIUM
®
Fenestrated Screw System is intended to be
used with the CONFIDENCE SPINAL CEMENT SYSTEM
®
or the
V-MAX™ Mixing and Delivery System and the VERTEBROPLASTIC
®
Radiopaque Resinous Material or the VERTECEM V+ Cement Kit
to provide immobilization and stabilization of spinal segments in
the treatment of acute and chronic instabilities or deformities of
the thoracic, lumbar and sacral spine in patients with diminished
bone quality (e.g., osteoporosis, osteopenia, metastatic disease).
It is intended to provide temporary internal support and fixation
while fusion mass is consolidating or fracture is healing, or for the
palliative reconstruction of the tumor patients.
CONTRAINDICATIONS
The use of EXPEDIUM Fenestrated Screw System is contraindi-
cated in patients presenting with any of the following conditions:
Disease conditions that have been shown to be safely and
predictably managed without the use of internal fixation devices
Acute compromise of the vertebral body or walls of the pedicles
and disruption of the posterior cortex
Anatomical damage of the vertebra that prevents safe screw
implantation
Active or incompletely treated infection
Coagulation disorders or severe cardiopulmonary disease
Haemorrhagic diasthesis
Spinal stenosis > 20% caused by retropulsed fragments
Vertebral body collapse to less than 1/3 (33%) original height
Coagulopathy or inability to reverse anti-coagulant therapy
(both during and approximately 24 hours post-procedure)
Allergic reaction to any of the components of the cement or
metal used
Relative contraindications include obesity, certain degenerative
diseases, and foreign body sensitivity. In addition, the patient’s
occupation or activity level or mental capacity may be relative
contraindications to this surgery. Specifically, patients who
because of their occupation or lifestyle, or because of conditions
such as mental illness, alcoholism, or drug abuse, may place
undue stresses on the implant during bony healing and may be
at higher risk for implant failure.
DESCRIPTION
The EXPEDIUM Fenestrated Screw System consists of Fenestrated
Screws and Clip-on Delivery System (includes a Cement Cannula
and a Clip). The EXPEDIUM Fenestrated Screw is a cannulated
polyaxial screw with fenestrations at the distal end of the screw
that are designed for cement introduction. The EXPEDIUM
Fenestrated Screw is designed for use in open and percutaneous
approaches and comes in a variety of sizes and lengths. It is
compatible for use with EXPEDIUM Spine Systems and VIPER
®
and VIPER
®
2 Spine Systems.
The EXPEDIUM Fenestrated Screw System can be used either
with the CONFIDENCE SPINAL CEMENT SYSTEM, or the
V-MAX Mixing and Delivery Device and the VERTEBROPLASTIC
Radiopaque Resinous Material, or the VERTECEM V+ Cement Kit.
When used with the CONFIDENCE SPINAL CEMENT SYSTEM,
EXPEDIUM Fenestrated Screw Cement Cannula must be
attached to the CONFIDENCE Spinal Cement Delivery System.
When used with the V-MAX Mixing and Delivery Device with the
VERTEBROPLASTIC Radiopaque Resinous Material, or the
VERTECEM V+ Cement, a CONFIDENCE Needle Adapter
(sold separately as an accessory to CONFIDENCE Spinal Cement
System) must be used to attach the V-MAX Flexible Tubing luer
lock to the Clip-on Delivery System.
2018-03-09 04:03:33

Table of Contents

Question and Answer IconNeed help?

Do you have a question about the Johnson & Johnson DePuy Synthes EXPEDIUM and is the answer not in the manual?

Johnson & Johnson DePuy Synthes EXPEDIUM Specifications

General IconGeneral
BrandJohnson & Johnson
ModelDePuy Synthes EXPEDIUM
CategoryMedical Equipment
LanguageEnglish

Summary

INDICATIONS FOR USE

CONTRAINDICATIONS

IMPORTANT INFORMATION

Please Read Before Use

Guidance to read and understand all provided information before product usage.

WARNINGS AND CAUTIONS

Limitations on Processing

Describes restrictions and limitations related to the processing of medical devices.

Point of Use Care

Instructions for immediate care of devices after surgical use to prevent soil drying.

Device Processing: Containment and Cleaning

Containment and Transportation

Guidelines for safely transporting used medical devices to the processing area.

Cleaning Preparation

Recommendations for preparing instruments and devices before initiating the cleaning process.

Manual Cleaning Method

Step-by-step instructions for manually cleaning medical devices using detergents.

Device Processing: Automated Steps

Automated Cleaning Cycle

Details of an automated washing cycle for medical devices, including rinse and wash phases.

Thermal Disinfection

Procedure for thermal disinfection using a washer-disinfector to ensure device safety.

Drying Process

Guidelines for drying medical devices, including automated and manual methods.

Device Maintenance and Sterilization

Manual Drying

Instructions for manually drying devices, focusing on surfaces and lumens.

Device Inspection Criteria

Key points to inspect for during device maintenance, including cleanliness and damage.

Sterilization Procedures

Recommended steam sterilization cycles and parameters for ensuring sterility.

Storage Guidelines

Recommendations for storing sterilized products in a clean and dry environment.

ADVERSE EVENTS

WARNINGS

PRECAUTIONS

PROCEDURE

IMPORTANT PHYSICIAN INFORMATION

LIMITED WARRANTY AND DISCLAIMER

SYMBOL TRANSLATION

Related product manuals