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Page 1: Surgical Technique and Product Catalog - Ortomedicortomedic.no/images/uploads/product_brochures/PerimeterSurgTech_(2... · Surgical Technique and Product Catalog FOR NON-USA USE ONLY

Surgical Technique and Product Catalog

FOR NON-USA USE ONLY

Page 2: Surgical Technique and Product Catalog - Ortomedicortomedic.no/images/uploads/product_brochures/PerimeterSurgTech_(2... · Surgical Technique and Product Catalog FOR NON-USA USE ONLY

INTRODUCTIONPercutaneous vertebroplasty and, more recently, kyphoplasty, are Vertebral Body Augmentation (VBA) procedures used for the treatment of painful vertebral compression fractures caused by osteoporosis, tumors or trauma.

Unlike other vertebroplasty or kyphoplasty systems that inject cement directly into the vertebral body, with the CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM®, the cement is injected into a mesh bag. This mesh bag provides additional control over placement of the cement. As the cement expands the mesh bag, there may also be the possibility of re-gaining some of the lost vertebral body height1, if the fracture is still mobile. The porous construction of the mesh allows the cement to extrude through the barrier and interdigitate with the surrounding cancellous bone. Additionally, it allows the bag to be removed once cement introduction is complete.

The CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM is only used in conjunction with the CONFIDENCE SPINAL CEMENT SYSTEM’s high viscosity cement and hydraulic delivery system.

For a complete list of warnings, precautions and contra-indications, please refer to the CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM Packaging Insert (IFU).

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CONTENTS

SURGICAL TECHNIQUE

·· Preparation 4

·· Bone Access Needle Placement 5

·· Biopsy Needle Placement (if required) 6

·· Bone Drill - Space Creation 7

·· Insertion of the Mesh Assembly 7

·· Cement Preparation 8

·· Cement Delivery 10

·· Retracting the Mesh Bag Assembly 13

·· Working Time and Temperature 13

·· CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM

Mesh Cutter Surgical Technique 14

PRODUCT CATALOG

·· CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM® 18

·· CONFIDENCE SPINAL CEMENT SYSTEM® 19

·· CONFIDENCE® Needleless Kit 20

INDICATIONS FOR USE

The CONFIDENCE PERIMETER SPINAL

CEMENT SYSTEM is indicated for use in

combination with the CONFIDENCE SPINAL

CEMENT SYSTEM. The CONFIDENCE

SPINAL CEMENT SYSTEM is intended for

percutaneous delivery of CONFIDENCE High

Viscosity Spinal Cement, which is indicated

for fixation of pathological fractures of the

vertebral body during vertebroplasty or

kyphoplasty procedures. Painful vertebral

compression fractures may result from

osteoporosis, benign lesions (haemangioma),

and malignant lesions (metastatic cancer,

myeloma).

NOTE:

The CONFIDENCE PERIMETER cement

injection cannula has a specifically designed

luer lock fitting. It is designed for use only

with CONFIDENCE SPINAL CEMENT SYSTEM

and the CONFIDENCE High Viscosity Spinal

Cement. The device is not compatible with

alternate materials.

NOTE:

A single CONFIDENCE SPINAL CEMENT

SYSTEM is restricted to be used with only one

CONFIDENCE PERIMETER SPINAL CEMENT

SYSTEM. When using a bilateral approach or

doing multiple levels with the CONFIDENCE

PERIMETER SPINAL CEMENT SYSTEM, a new

CONFIDENCE SPINAL CEMENT SYSTEM should

be opened and used for each level/approach.

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Vertebral Body Augmentation

4

SURGICAL TECHNIQUE

PATIENT POSITIONING AND PREPARATION

The patient should be in a prone position on a radiolucent table, permitting AP and lateral imaging using uni or bi-planar x-ray and/or CT. Either local or general anaesthesia may be used. Prepare the operative site according to standard surgical techniques and hospital procedures.

INSTRUMENT PREPARATION

The bone access needle is packaged with a beveled tip stylet. If a diamond tip is preferred, remove the beveled stylet and replace with the diamond stylet. Ensure that the diamond stylet is adequately locked to the handle of the access needle.

The mesh needle assembly should not be disassembled. Disassembly will lead to disengagement of the stylet from the mesh bag which may result in piercing of the mesh bag when reinserted.

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5

Surgical Technique

BONE ACCESS NEEDLE PLACEMENT

Under fluoroscopy, insert the bone access needle (working cannula and stylet) down to the appropriate entry location to the vertebral body. The trajectory by which the needle is inserted varies depending on the vertebra to be treated. Most commonly a transpedicular or extrapedicular approach is performed. A uni-pedicular or bi-pedicular approach may be used at the operator’s discretion.

Using alternating A/P and lateral fluoroscopy, the needle can be guided into the vertebral body. The tip of the needle should commonly begin superior and lateral to the border of the pedicle on an A/P image. The needle is advanced, under lateral fluoroscopy, into the vertebral body. During needle advancement, great care should be taken to avoid breaching the medial border of the pedicle. This is accomplished by checking that when the tip of the needle on lateral fluoroscopy is flush with the posterior border of the vertebral body, that it is not medial to the medial border of the pedicle on the A/P image.

NOTE:

Care should be taken to

position the distal tip of the

working cannula to allow

space for the CONFIDENCE

PERIMETER Mesh Bag (23mm

beyond the distal tip).

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Vertebral Body Augmentation

6

The needle holder, in combination with the long-armed mallet, may be used to position and advance the needle under fluoroscopy, while keeping the physician’s hands outside the x-ray field.

After passing the vertebral posterior wall using the CONFIDENCE PERIMETER bone access needle, hold the working cannula firmly in place and remove the stylet.

BIOPSY NEEDLE PLACEMENT (IF REQUIRED)

Under fluoroscopy and/or CT guidance, insert the CONFIDENCE biopsy needle through the bone access needle for biopsy collection. According to the user’s preference in biopsy technique, the stylet may be removed either before insertion of the biopsy needle, or after the vertebral posterior wall has been passed.

NOTE:

In case of beveled tip needles,

the arrows on the handle

of the needle point to the

direction of the bevel.

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7

Surgical Technique

BONE DRILL - SPACE CREATION

Under fluoroscopy and/or CT guidance, fully insert the bone drill through the working cannula, using a clockwise, rotating motion. This will create a working space for the mesh bag. When the bone drill is fully inserted through the working cannula, the distal tip of the drill represents the location of the distal tip of the mesh bag. Attention should be paid not to breach the anterior wall of the vertebral body while advancing the bone drill. Once completed, remove the drill.

INSERTION OF THE MESH ASSEMBLY

Under fluoroscopy and/or CT guidance, insert the mesh assembly through the working cannula until it is firmly attached to the handle of the working cannula.

While firmly holding the working cannula’s handle, remove the mesh assembly stylet using a counter-clockwise rotation.

NOTE:

If the predicted location of

the mesh bag (indicated by

the location of the drill tip)

is unsatisfactory, re-position

the working cannula and drill

prior to insertion of the mesh

assembly.

NOTE:

To prevent advancement of

the working cannula, firmly

hold the cannula in place while

inserting the mesh assembly.

Insert the mesh assembly into

the working cannula using

a uni-directional motion.

Withdrawal and re-insertion

may cause the stylet’s tip to

disengage from the tip of

the mesh bag and potentially

pierce the bag.

NOTE:

The CONFIDENCE PERIMETER

cement injection cannula has a

specifically designed luer lock

fitting. It is designed for use

only with CONFIDENCE SPINAL

CEMENT SYSTEM and the

CONFIDENCE High Viscosity

Spinal Cement. The device is

not compatible with alternate

materials.

NOTE:

Once removed, do not reinsert

stylet as it may result in

piercing of the mesh bag.

Mesh bag tip

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Vertebral Body Augmentation

8

CEMENT PREPARATION

Pour the entire contents of the cement powder into the mixing bowl. Pour the entire contents of the liquid monomer vial over the cement powder in the mixing bowl.

WORKING TIME AND TEMPERATURE

While holding the mixing bowl vertically on the table, push down on the outer ring of the mixer handle and screw this ring onto the mixing bowl in a clockwise direction.

NOTE:

Prior to cement mixing, ensure

that the mesh assembly is in

its final position. Important:

CONFIDENCE PERIMETER

working time = cement

mixing, transfer, injection and

mesh bag retraction.

NOTE:

Powder should always be

poured into the mixing bowl

first. Care should be taken not

to open the liquid monomer

vial over the mixing bowl

due to risk of glass splinters.

Important: Timings provided

begin at start of mixing.

NOTE:

Prior to introducing the mixer

handle into the mixing bowl,

verify that the wiper blade is

attached to the inside of the

mixer handle. If it is not, attach

the wiper blade to the mixer

handle by snapping it into

place. Keep in mind that the

teeth should point upwards.

Important: Closely monitor

the working time of the

procedure (see chart above). wiper blade

Theatre Temperature (°C)

End of Working Time (Cement mixing, transfer, injection and mesh bag retraction)

Start of Setting Time(Working cannula removal)

18° 7 minutes 14 minutes

22° 6 minutes 12 minutes

25° 5 minutes 10 minutes

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9

Surgical Technique

Mix the cement by turning the handle 3 turns in one direction, then 3 turns in the opposite direction. Repeat for a total of 40-60 seconds.

Unscrew the ring on the mixer handle in a counter-clockwise direction and remove the handle from the mixing bowl. The cement and wiper blade will remain in the mixing bowl.

Push and screw the cement reservoir adaptor onto the mixing bowl with a clockwise rotation until firmly seated in the bottom of the bowl. This process will force the cement into the cement reservoir. Ensure that the cement is fully distributed to the distal tip of the reservoir.

Unscrew the cement reservoir from the cement reservoir adaptor with a counter-clockwise rotation.

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Vertebral Body Augmentation

10

CEMENT DELIVERY

Screw the cement reservoir cap securely onto the cement reservoir. Care should be taken to align the cap carefully with the threaded reservoir to ensure proper thread engagement. It is important that the cap is fully tightened before pressurizing or delivering cement. A small amount of cement may extrude from the tip and should be removed before assembly to the needle.

Connect the hydraulic pump’s flexible tube to the cement reservoir cap by pushing and snapping the quick-connect assembly onto the cement reservoir cap.

NOTE:

Ensure the piston inside the

cap is properly attached to the

cap before threading onto the

reservoir. The reservoir cap

must be fully seated against

the flange on the cement

reservoir.

NOTE:

If the quick connect will not

attach to the reservoir cap,

rotate the handle of the pump

counter-clockwise to relieve

some pressure. This will allow

the connector to attach to

the cap.

cap flange

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11

Surgical Technique

Screw the reservoir tip onto the luer fitting of the mesh assembly cement injection cannula (white in color). Keep hold of the working cannula to prevent advancing it further into the vertebral body.

Prepare the system for delivery by turning the pump handle a few turns, until a small amount of cement extrudes into the mesh bag. This should be done under fluoroscopic guidance. While monitoring the mesh bag under fluoroscopy, slowly rotate the pump handle clockwise half a turn per second until cement begins to fill the mesh bag.

Each half turn (180 degrees) of the handle will inject approximately 0.15 ml/cc of cement. As the cement is introduced, the CONFIDENCE PERIMETER mesh bag will expand within the vertebral body. It takes approximately 2 ml/cc of cement to fully expand the bag.

NOTE:

Care must be taken to avoid

overtightening the cement

reservoir to the mesh assembly

(white luer).

NOTE:

The hydraulic pump has

a safety release valve that

restricts the build-up of excess

pressure in the reservoir. The

scale on the cement reservoir

is intended to approximate the

amount of cement introduced.

Fluoroscopy should be used to

confirm the correct amount

of cement introduced into

the vertebral body. Note

that the volume of cement

in the injection cannula is

approximately 0.3ml.

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Vertebral Body Augmentation

12

Cement can continue to be introduced and will extrude through the pores of the mesh bag and interdigitate with the surrounding bone structure.

When cement introduction is complete, rotate the pump handle counter-clockwise until pump handle spins freely to depressurize the cement reservoir. While firmly holding the injection cannula cap (white in color) in one hand, disconnect the cement reservoir from the mesh assembly.

Firmly hold the working cannula’s handle (blue in color) and remove the injection cannula (white in color) from the mesh assembly, using a counter-clockwise rotation.

NOTE:

Upon completion, or at any

point during the procedure,

cement flow can be stopped

by rapidly rotating the handle

counter-clockwise until pump

handle spins freely.

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13

Surgical Technique Guide

RETRACTING THE MESH BAG ASSEMBLY

Flip up the winding handle on the mesh assembly (grey in color).

Rotate the winding handle 3-4 full 360° turns until the mesh bag is completely retracted into the working cannula. Confirm that this step is complete using fluoroscopy.

Prior to the start of the cement setting time (see chart below), remove the working cannula/mesh assembly from the vertebral body by rotating and pulling the cannula. This will allow easier removal of the cannula. The needle introduction site can be closed with a single suture, a steri-strip, or in any other manner preferred by the operator.

WORKING TIME AND TEMPERATURE

Theatre Temperature (°C)

End of Working Time (Cement mixing, transfer, injection and mesh bag retraction)

Start of Setting Time(Working cannula removal)

18° 7 minutes 14 minutes

22° 6 minutes 12 minutes

25° 5 minutes 10 minutes

Please note that mesh bag is intended to be retrieved and working times in Time/Temperature Table should be followed carefully to retrieve the mesh bag during the required retraction time period. If the physician encounters a situation where they are unable to retrieve the mesh bag for any reason, or if it is in the best interest of the patient to keep the mesh bag in place, the following steps should be taken:

1. Pull out the winding handle from the mesh assembly.2. Remove the working cannula.3. Open skin incision to accept PERIMETER Mesh Cutter, if necessary.4. Clamp onto the tail of the mesh bag and run the cutting tool (e.g. surgical scissors) down

the length of the mesh bag.5. Cut the mesh bag as close to the pedicle as possible and close the incision.

NOTE:

Ensure removal of the mesh

bag from the vertebral body

prior to the end of the cement

working time. (see chart below).

NOTE:

The CONFIDENCE PERIMETER

SPINAL CEMENT SYSTEM

must be stored at temperatures

between 5°C (41°F) to

25°C (77°F).

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14

Vertebral Body Augmentation

PERIMETER MESH CUTTER SURGICAL TECHNIQUE

Please note that mesh bag is intended to be retrieved and working times in Time/TemperatureTable should be followed carefully to retrieve the mesh bag during the required retraction timeperiod. If the physician encounters a situation where they are unable to retrieve the mesh bagfor any reason, or if it is in the best interest of the patient to keep the mesh bag in place, the following steps should be taken:

1. Pull out the winding handle from the mesh assembly.

2. Remove the working cannula from the patient.

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Surgical Technique Guide

15

3. Open skin incision as needed to accept the PERIMETER Mesh Cutter.

4. Insert end of mesh bag into the slot of PERIMETER Mesh Cutter tip.

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16

Vertebral Body Augmentation

5. Hold on to end of mesh bag while advancing PERIMETER Mesh Cutter along mesh bag until the Mesh Cutter contacts vertebral body.

Use flouro to verify that PERIMETER Mesh Cutter is at the pedicle.

6. Cut the mesh bag as close to the pedicle as possible.

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Surgical Technique Guide

17

7. Remove PERIMETER Mesh Cutter and end of mesh bag from patient.

8. Close the incision.

NOTE:

If desired, distal tip of working

cannula stylet can be used to

pack any protruding mesh

into pedicle.

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Vertebral Body Augmentation

18

PRODUCT CATALOG

CONFIDENCE PERIMETER KIT / CATALOG NO. 2839-22-000

Components included in kit:

• Bone Access Needle/Working Cannula, Beveled Tip, 11G, 100mm

• Additional Stylet, Diamond tip, 11G, 100mm

• Bone Drill

• Mesh Assembly

Component DescriptionsBone Access Needle/Working CannulaConsists of a working cannula and a beveled tip stylet for percutaneous bone access. The needle also acts as a cannula through which the bone drill and PERIMETER Mesh Assembly are introduced into the vertebra.

Stylet - Diamond TipThe beveled tip stylet in the introducer needle can be removed and replaced with the diamond tip stylet, if preferred.

Bone DrillInserted through the working cannula to create a working space for the introduction of the CONFIDENCE PERIMETER Mesh Assembly within the vertebral body.

CONFIDENCE PERIMETER Mesh AssemblyConsists of the mesh bag, an injection needle assembly and a blunt tip stylet. The mesh bag is made from a porous fabric and is equipped with a winding handle at its proximal end. It protrudes 23mm beyond the working cannula. Cement is introduced into the mesh bag through a small diameter injection cannula.

PERIMETER MESH CUTTER / CATALOG NO. 2839-22-500

MESH CUTTER CASE / CATALOG NO. 2839-22-600

Advance mesh cutter along the mesh bag until the mesh cutter contacts vertebral body. Then cut the mesh bag as close to the pedicle as possible.

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19

Product Catalog

CONFIDENCE PLUS KIT / CATALOG NO. 2839-10-000

Components included in kit:

• CONFIDENCE High Viscosity Spinal Cement (11ml)

• Hydraulic Pump

• Cement Reservoir & Mixer

• Mallet & Needle Holder

• 2 Introducer Needles, Diamond Tip, 13G, 100mm

• Biopsy Needle, 15G, 230mm CONFIDENCE High Viscosity Spinal Cement (11ml)

Component DescriptionsCONFIDENCE High Viscosity Spinal CementConsists of a ampoule of liquid monomer and a packet of powder polymer. Mixing the 2 components for 40 – 60 seconds results in a high viscosity, radiopaque cement. This high viscosity texture allows for an 8 – 10 minutes at 68F (20C), and enables a controlled introduction of cement.

Hydraulic PumpThe hydraulic pump enables a smooth and effortless introduction of highly viscous cement into the vertebra. It is provided pre-filled with sterile water. Its flexible extension tube enables the physician to keep his/her hands outside of the direct fluoroscopy exposure field.

Cement MixerConsisting of a mixing bowl and mixer handle, this unique, closed mixer enables easy mixing of the cement.

Cement Reservoir & Cement Reservoir AdaptorThe cement reservoir is an 11 ml/cc transparent barrel with volumetric reference markings. The cement reservoir adaptor enables the transfer of the cement into the cement reservoir following mixing.

Long Handled Radiolucent MalletA long handled, 150-gram disposable mallet to aid in needle introduction. The long radiolucent handle allows the physician to tap the needle during fluoroscopy, while keeping his/her hands outside of the direct fluoroscopy field.

Needle HolderRadiolucent needle holder, allowing for manipulation of needle placement while keeping the hands of the physician outside the direct fluoroscopy field.

Introducer Needle, Diamond Tip, 13G, 100mmConsists of a needle and a stylet for bone access. The needle also acts as a cannula through which the cement is introduced into the vertebra.

Biopsy Needle, 15G, 230mmThe biopsy needle consists of a needle and stylet intended for use through an 11 gauge or 13 gauge introducer needle.

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Vertebral Body Augmentation

20

CONFIDENCE NEEDLELESS KIT / CATALOG NO. 2839-13-000

Components included in kit:

• CONFIDENCE High Viscosity Spinal Cement (11ml)

• Hydraulic Pump

• Cement Reservoir & Mixer

• Mallet & Needle Holder

Component DescriptionsCONFIDENCE High Viscosity Spinal CementConsists of a ampoule of liquid monomer and a packet of powder polymer. Mixing the 2 components for 40 – 60 seconds results in a high viscosity, radiopaque cement. This high viscosity texture allows for an 8 – 10 minutes at 68F (20C), and enables a controlled introduction of cement.

Hydraulic PumpThe hydraulic pump enables a smooth and effortless introduction of highly viscous cement into the vertebra. It is provided pre-filled with sterile water. Its flexible extension tube enables the physician to keep his/her hands outside of the direct fluoroscopy exposure field.

Cement MixerConsisting of a mixing bowl and mixer handle, this unique, closed mixer enables easy mixing of the cement.

Cement Reservoir & Cement Reservoir AdaptorThe cement reservoir is an 11 ml/cc transparent barrel with volumetric reference markings. The cement reservoir adaptor enables the transfer of the cement into the cement reservoir following mixing.

Long Handled Radiolucent MalletA long handled, 150-gram disposable mallet to aid in needle introduction. The long radiolucent handle allows the physician to tap the needle during fluoroscopy, while keeping his/her hands outside of the direct fluoroscopy field.

Needle HolderRadiolucent needle holder, allowing for manipulation of needle placement while keeping the hands of the physician outside the direct fluoroscopy field.

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CONFIDENCE NEEDLELESS KIT / CATALOG NO. 2839-07-000

Components included in kit:

• CONFIDENCE High Viscosity Spinal Cement (7cc)

• Hydraulic Pump

• Cement Reservoir & Mixer

Component DescriptionsCONFIDENCE High Viscosity Spinal CementConsists of a ampoule of liquid monomer and a packet of powder polymer. Mixing the 2 components for 40 – 60 seconds results in a high viscosity, radiopaque cement. This high viscosity texture allows for an 8 – 10 minutes at 68F (20C), and enables a controlled introduction of cement.

Hydraulic PumpThe hydraulic pump enables a smooth and effortless introduction of highly viscous cement into the vertebra. It is provided pre-filled with sterile water. Its flexible extension tube enables the physician to keep his/her hands outside of the direct fluoroscopy exposure field.

Cement MixerConsisting of a mixing bowl and mixer handle, this unique, closed mixer enables easy mixing of the cement.

Cement Reservoir & Cement Reservoir AdaptorThe cement reservoir is an 11 ml/cc transparent barrel with volumetric reference markings. The cement reservoir adaptor enables the transfer of the cement into the cement reservoir following mixing.

21

Product Catalog

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22

Vertebral Body Augmentation

NOTES

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Surgical Technique Guide

23

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© DePuy Spine, Inc. 2010. All rights reserved.

ADDB/UM 09/10

Not all products are currently available in all markets.

DePuy Spine EMEA is a trading division of DePuy International Ltd. DePuy International Ltd. • DePuy France SAS • DePuy Orthopädie GmbH Registered office: St. Anthony’s Road, Leeds LS11 8DT, England Registered in England No. 3319712

DePuy International Ltd.St. Anthony’s Road Leeds LS11 8DTEnglandTel: +44 (0) 113 387 7800Fax: +44 (0) 113 387 7890

www.depuy.com

30%

Reference:1. An Ex Vivo Biomechanical Evaluation of the CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM® used in the Treatment of Compression Fractures. White Paper, DePuy SpineTM, 2009. (Re-order code 9084-61-000)

FOR NON-USA USE ONLY

INDICATIONS

The CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM® is indicated for use in combination with the CONFIDENCE SPINAL CEMENT SYSTEM®. The CONFIDENCE SPINAL CEMENT SYSTEM is intended for percutaneous delivery of CONFIDENCE High Viscosity Spinal Cement, which is indicated for fixation of pathological fractures of the vertebral body during vertebroplasty or kyphoplasty procedures. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancer, myeloma).

CONTRAINDICATIONS

The use of CONFIDENCE PERIMETER SPINAL CEMENT SYSTEM is contraindicated in patients presenting with any of the following conditions:

• Use of CONFIDENCE High Viscosity Spinal Cement for prophylaxis (such as in metastatic or osteoporotic patients with no evidence of acute vertebral fracture). • Coagulation disorders, or severe cardiopulmonary disease. • Haemorrhagic diasthesis. • Non-pathological, acute, traumatic fractures of the vertebra. • Patient clearly improving on medical therapy. • Spinal stenosis (>20% by retropulsed fragments). • Compromise of the vertebral body or walls of the pedicles. • Compromise or instability of vertebral fractures due to posterior involvement. • Anatomical damage of the vertebra that prevents safe access of the needle to the vertebral body. • Vertebral body collapse to less than 1/3 (33%) original height. • Vertebral plana (collapse >90%). • Active or incompletely treated infection. • Coagulopathy or inability to reverse anti-coagulant therapy (both during and approximately 24 hours post-procedure). • Severe pulmonary insufficiency. • Allergic reaction to any of the components of the CONFIDENCE High Viscosity Spinal Cement.

Limited Warranty and Disclaimer: DePuy Spine products are sold with a limited warranty to the original purchaser against defects in workmanship and materials. Any other express or implied warranties, including warranties of merchantability or fitness, are hereby disclaimed.