MEDIVISION, INC. MVA470S MEDIVISION

Set includes the following: Stryker Items: 3910-500-727 Suture Manipulator 3910-500-742 Suture Cutter 2mm 3910-500-739 Penetrating Grasper 45* 3910-500-738 Penetrating Grasper 30* 3910-500-737 Penetrating Grasper Str. 3910-500-736 Penetrating Grasper L 3910-500-735 Penetrating Grasper R 3910-500-850 5mm Probe x2 3910-500-733 Tissue Liberator Blade Up 3910-500-734 Tissue Liberator Blade Down 3910-500-732 Rasp Down Bend Arthrex Items: AR-13970SR KingFisher Suture Retriever/Tissue Grasper with SR Handle AR-13974SR FiberTape Retriever with SR Handle, Self-Ratcheting AR-11794L Suture Cutter, 4.2 mm, Open-End, Left Notch (Used w/ All Suture) AR-13250 FiberTape Suture Cutter

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s). An access channel is required for the Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to it's start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.

VULCAN EFLEX ABLATOR ABLATOR PROBE WITH INTEGRATED CABLE

Outflow Cassette Tubing, Do not use if package is damaged

DW OUTFLOW CASSETTE/TUBE SET

FMS Fluid Management System Intermediary Tubing with One-way valve

AR-11910SR: Grasper, Mini Straight Tip, ø2.75 mm 15° Up Curved Shaft w/SR Handle AR-13600SR: Grasper, Alligator Hook Tip, ø4.2 mm, Straight Shaft w/SR Handle AR-12500SR: Grasper, Blunt Straight Tip, ø3.4 mm Straight Shaft w/SR Handle AR-11200: Punch, Large 2.75 mm, Straight Shaft AR-12000: Punch, Standard Straight Tip, ø3.4 mm Straight Shaft AR-12240: Punch, WideBiter 15° Up Tip, ø3.4 mm Straight Shaft AR-12241: Punch, WideBiter 15° Up Tip, ø3.4 mm 15° Up Curved Shaft AR-12530: Punch, Medium Reverse Straight Tip, ø3.4 mm Straight Shaft AR-12800: Punch, Medium 45° Right Angled Tip, ø3.4 mm Straight Shaft AR-12810: Punch, Medium 45° Left Angled Tip, ø3.4 mm Straight Shaft AR-12912: Punch, WideBiter 90° Right Rotary Tip, 3.4 mm Straight Shaft AR-12913: Punch, WideBiter Rotary 90° Left Tip, ø3.4 mm Straight Shaft AR-12950: Punch, Rotary with Scoop 90° Left Tip, ø3.4 mm Straight Shaft AR-12940: Punch, Rotary with Scoop 90° Right Tip, ø3.4 mm Straight Shaft

Set includes the following: Stryker Items: 3910-500-727 Suture Manipulator 3910-500-742 Suture Cutter 2mm 3910-500-739 Penetrating Grasper 45* 3910-500-738 Penetrating Grasper 30* 3910-500-737 Penetrating Grasper Str. 3910-500-736 Penetrating Grasper L 3910-500-735 Penetrating Grasper R 3910-500-850 5mm Probe x2 3910-500-733 Tissue Liberator Blade Up 3910-500-734 Tissue Liberator Blade Down 3910-500-732 Rasp Down Bend Arthrex Items: AR-13970SR KingFisher Suture Retriever/Tissue Grasper with SR Handle AR-13974SR FiberTape Retriever with SR Handle, Self-Ratcheting AR-11794L Suture Cutter, 4.2 mm, Open-End, Left Notch (Used w/ All Suture) AR-13250 FiberTape Suture Cutter

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s). An access channel is required for the Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to it's start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.