| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00813478020070 | PLT1910 | PLT1910 | Kiva Pilot, Left | OCJ | Spinal Channeling Instrument, Vertebroplasty | 1 | Kiva |
| 2 | 00813478020438 | MS3101 | MS3101 | Verterbral Augmentation Cement | NDN | Cement, Bone, Vertebroplasty | 2 | Kiva |
| 3 | 00813478020414 | MS3643 | MS3643 | Mixing and Injection System | OAR | Injector, Vertebroplasty (Does Not Contain Cement) | 1 | Kiva |
| 4 | 00813478020407 | ACC5350 | ACC5350 | Kiva UltraFlex Cement Needle Kit | GAA | Needle, Aspiration And Injection, Disposable | 1 | Kiva |
| 5 | 00813478020179 | VAK1800 | VAK1800 | Vertebral Augmentation Cement Kit for Use with Kiva | NDN,OAR | Cement, Bone, Vertebroplasty,Injector, Vertebroplasty (Does Not Contain Cement) | 1 | Kiva |
| 6 | 00813478020162 | ACC5270 | ACC5270 | Kiva Introducer Set | GEA | Cannula, Surgical, General & Plastic Surgery | 1 | Kiva |
| 7 | 00813478020155 | ACC5260 | ACC5260 | Kiva Trocar Tip Access Needle, 11GA | GAH | Stylet, Surgical, General & Plastic Surgery | 1 | Kiva |
| 8 | 00813478020148 | ACC5250 | ACC5250 | Kiva Cement Needle Set | GAA | Needle, Aspiration And Injection, Disposable | 1 | Kiva |
| 9 | 00813478020131 | ACC5240 | ACC5240 | Kiva Bevel Tip Access Needle, 11GA | GAH | Stylet, Surgical, General & Plastic Surgery | 1 | Kiva |
| 10 | 00813478020124 | ACC5230 | ACC5230 | Kiva Diamond Tip Access Needle, 11GA | GAH | Stylet, Surgical, General & Plastic Surgery | 1 | Kiva |
| 11 | 00813478020117 | ACC5225 | ACC5225 | Bone Drill, 7GA x 17cm | HTW | Bit, Drill | 1 | Kiva |
| 12 | 00813478020100 | ACC5220 | ACC5220 | Bone Drill, 7GA x 19cm | HTW | Bit, Drill | 1 | Kiva |
| 13 | 00813478020094 | ACC1520 | ACC1520 | CorePlus Bone Biopsy Needle, 11GA | GAA | Needle, Aspiration And Injection, Disposable | 1 | Kiva |
| 14 | 00813478020087 | ACC1510 | ACC1510 | CorePlus Bone Biopsy Needle, 15GA | GAA | Needle, Aspiration And Injection, Disposable | 1 | Kiva |
| 15 | 00813478020063 | PLT1900 | PLT1900 | Kiva Pilot, Right | OCJ | Spinal Channeling Instrument, Vertebroplasty | 1 | Kiva |
| 16 | 00813478020056 | FRS2200 | FRS2200 | Kiva VCF Treatment System, First Fracture, Left | LOD,NDN | Bone Cement,Cement, Bone, Vertebroplasty | 2 | Kiva |
| 17 | 00813478020049 | FRS2100 | FRS2100 | Kiva VCF Treatment System, First Fracture, Right | LOD,NDN | Bone Cement,Cement, Bone, Vertebroplasty | 2 | Kiva |
| 18 | 00813478020032 | KIV2250 | KIV2250 | Kiva VCF Treatment System, Additional Fracture Kit, Left | LOD,NDN | Bone Cement,Cement, Bone, Vertebroplasty | 2 | Kiva |
| 19 | 00813478020025 | KIV2200 | KIV2200 | Kiva VCF Treatment System, First Fracture Kit, Left | LOD,NDN | Bone Cement,Cement, Bone, Vertebroplasty | 2 | Kiva |
| 20 | 00813478020018 | KIV2150 | KIV2150 | Kiva VCF Treatment System, Additional Fracture Kit, Right | LOD,NDN | Bone Cement,Cement, Bone, Vertebroplasty | 2 | Kiva |
| 21 | 00813478020001 | KIV2100 | KIV2100 | Kiva VCF Treatment System, Fisrt Fracture Kit, Right | LOD,NDN | Bone Cement,Cement, Bone, Vertebroplasty | 2 | Kiva |
| 22 | 00813478020391 | LUN4200 | LUN4200 | Luna 3D Lordotic Accessory Kit | LXH | Orthopedic Manual Surgical Instrument | 1 | Luna 3D |
| 23 | 00813478020384 | LUN4001 | LUN4001 | Luna 3D Graft Injector Tool, Disposable | LXH | Orthopedic Manual Surgical Instrument | 1 | Luna 3D |
| 24 | 00813478020421 | MS2079 | MS2079 | F20 Radiopaque Bone Cement | NDN | Cement, Bone, Vertebroplasty | 2 | Blazer |
| 25 | 00813478020377 | LUN4000 | LUN4000 | Luna 3D Accessory Kit | LXH | Orthopedic Manual Surgical Instrument | 1 | Luna 3D |
| 26 | 00813478020360 | LUN3015-08 | LUN3015-08 | 15mm, 8-Degree, Luna 3D Lordotic Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 27 | 00813478020353 | LUN3014-08 | LUN3014-08 | 14mm, 8-Degree, Luna 3D Lordotic Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 28 | 00813478020346 | LUN3013-08 | LUN3013-08 | 13mm, 8-Degree, Luna 3D Lordotic Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 29 | 00813478020339 | LUN3012-08 | LUN3012-08 | 12mm, 8-Degree, Luna 3D Lordotic Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 30 | 00813478020322 | LUN3011-08 | LUN3011-08 | 11mm, 8-Degree, Luna 3D Lordotic Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 31 | 00813478020315 | LUN3010-08 | LUN3010-08 | 10mm, 8-Degree, Luna 3D Lordotic Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 32 | 00813478020308 | LUN3013 | LUN3013 | 13mm Luna 3D Parallel Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 33 | 00813478020292 | LUN3012 | LUN3012 | 12mm Luna 3D Parallel Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 34 | 00813478020285 | LUN3011 | LUN3011 | 11mm Luna 3D Parallel Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 35 | 00813478020278 | LUN3010 | LUN3010 | 10mm Luna 3D Parallel Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 36 | 00813478020261 | LUN3009 | LUN3009 | 9mm Luna 3D Parallel Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 37 | 00813478020254 | LUN3008 | LUN3008 | 8mm Luna 3D Parallel Implant Kit | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Luna 3D |
| 38 | 00813478020230 | ACC3150 | ACC3150 | Blazer Cement Needle, 11GA | GAA | Needle, Aspiration And Injection, Disposable | 1 | Blazer |
| 39 | 00813478020223 | ACC3140 | ACC3140 | Blazer Single Step Bevel Tip Introducer | GAH | Stylet, Surgical, General & Plastic Surgery | 1 | Blazer |
| 40 | 00813478020216 | ACC3130 | ACC3130 | Blazer Single Step Diamond Trocar Tip Introducer | GAH | Stylet, Surgical, General & Plastic Surgery | 1 | Blazer |
| 41 | 00813478020209 | ACC3120 | ACC3120 | Blazer Bone Drill | HTW | Bit, Drill | 1 | Blazer |
| 42 | 00813478020193 | BZK3130 | BZK3130 | Blazer-C Vertebral Augmentation Kit | OCJ | Spinal Channeling Instrument, Vertebroplasty | 1 | Blazer |
| 43 | 00813478020186 | BCN3120 | BCN3120 | Blazer-C Vertebral Augmentation System | OCJ | Spinal Channeling Instrument, Vertebroplasty | 1 | Blazer |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | B330OT02240 | OT-0224 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves 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. 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 its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Straight Balloon (10ga/4ml) | OSSEON LLC | |
| 2 | B330OT02220 | OT-0222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves 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. 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 its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Straight Balloon (10ga/2ml) | OSSEON LLC | |
| 3 | B330OF82220 | OF-8222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves 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. | Osseoflex SB Steerable Balloon (8ga/2ml) | OSSEON LLC | |
| 4 | B330OF02240 | OF-0224 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves 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.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 its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon ( 10 ga/ 4ml) | OSSEON LLC | |
| 5 | B330OF02220 | OF-0222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves 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. | Osseoflex SB Steerable Balloon (10ga/2ml) | OSSEON LLC | |
| 6 | B330OF00050 | OF-0005 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves 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. | Osseoflex SB Steerable Balloon (8ga/ 4ml) | OSSEON LLC | |
| 7 | 30808232001137 | 2110-0507 | 2110-0507 | Flexible Extensions | Aliquot | STRYKER CORPORATION |
| 8 | 30808232000949 | 2110-0031 | 2110-0031 | Mix Tips, Luer | Cortoss | STRYKER CORPORATION |
| 9 | 28031497002006 | ASC0030 | Mendec Aqua Cartridge is intended to be used with Mendec Aqua in vertebral augme Mendec Aqua Cartridge is intended to be used with Mendec Aqua in vertebral augmentation procedure (vertebroplasty, kyphoplasty and screw-augmentation) when the acrylic resin/bone void filler loaded in a single cartridge is not sufficient to complete the surgical procedure. | MENDEC AQUA CARTRIDGE | TECRES SPA | |
| 10 | 28031497001702 | ASC0020 | MENDEC AQUA is a sterile single-use device for extrusion into the bone of acryli MENDEC AQUA is a sterile single-use device for extrusion into the bone of acrylic resins or bone void fillers (not supplied with the kit) intended for vertebral augmentation procedures (vertebroplasty, kyphoplasty, screw-augmentation). | MENDEC AQUA | TECRES SPA | |
| 11 | 28031497001382 | 13C2040 | Mendec Spine HV System is indicated for the treatment of pathological fractures Mendec Spine HV System is indicated for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure.Mendec Spine HV System is a closed sysyem which containes the powder and liquid components separately.The device is disposable and sterile. | Mendec Spine HV System | TECRES SPA | |
| 12 | 28031497000521 | 13C2000 | Mendec Spine Kit is a device for the treatment of pathological fractures of the Mendec Spine Kit is a device for the treatment of pathological fractures of the vertebral body using a vertebroplasty procedure.The device is composed by an acrylic resin and a delivery system. | Mendec Spine Kit | TECRES SPA | |
| 13 | 28031497000101 | 1230 | Mendec Spine is an acrylic resin for the treatment of pathological fractures of Mendec Spine is an acrylic resin for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure.Mendec Spine is a medium-high viscosity acrylic resin (PMMA-based), highly radiopaque for syringe application.The device is sold disposable and sterile | Mendec Spine | TECRES SPA | |
| 14 | 15056033810538 | INTV-CEM | Osteoflex | PAN MEDICAL US CORPORATION | ||
| 15 | 10888857530096 | PRO-1117-06 | PRO-1117-06 | Tap, Fenestrated Size Ø8.5 | K2M Fenestrated Tap System | K2M, INC. |
| 16 | 10888857530089 | PRO-1117-05 | PRO-1117-05 | Tap, Fenestrated Size Ø7.5 | K2M Fenestrated Tap System | K2M, INC. |
| 17 | 10888857530072 | PRO-1117-04 | PRO-1117-04 | Tap, Fenestrated Size Ø6.5 | K2M Fenestrated Tap System | K2M, INC. |
| 18 | 10888857530065 | PRO-1117-03 | PRO-1117-03 | Tap, Fenestrated Size Ø5.5 | K2M Fenestrated Tap System | K2M, INC. |
| 19 | 10888857530058 | PRO-1117-02 | PRO-1117-02 | Tap, Fenestrated Size Ø4.5 | K2M Fenestrated Tap System | K2M, INC. |
| 20 | 10888857530041 | PRO-1117-01 | PRO-1117-01 | Tap, Fenestrated Size Ø4.0 | K2M Fenestrated Tap System | K2M, INC. |
| 21 | 10888857461338 | SP-4029-06 | SP-4029-06 | Tap, Fenestrated, Size Ø8.5 | K2M Fenestrated Tap System | K2M, INC. |
| 22 | 10888857461321 | SP-4029-05 | SP-4029-05 | Tap, Fenestrated, Size Ø7.5 | K2M Fenestrated Tap System | K2M, INC. |
| 23 | 10888857461314 | SP-4029-04 | SP-4029-04 | Tap, Fenestrated, Size Ø6.5 | K2M Fenestrated Tap System | K2M, INC. |
| 24 | 10888857461307 | SP-4029-03 | SP-4029-03 | Tap, Fenestrated, Size Ø5.5 | K2M Fenestrated Tap System | K2M, INC. |
| 25 | 10888857461291 | SP-4029-02 | SP-4029-02 | Tap, Fenestrated, Size Ø4.5 | K2M Fenestrated Tap System | K2M, INC. |
| 26 | 10888857461284 | SP-4029-01 | SP-4029-01 | Tap, Fenestrated, Size Ø3.5 | K2M Fenestrated Tap System | K2M, INC. |
| 27 | 10888857183148 | 5001-90017 | 5001-90017 | Tap, Fenestrated, Size Ø8.5 mm | K2M Fenestrated Tap System | K2M, INC. |
| 28 | 10888857183131 | 5001-90016 | 5001-90016 | Tap, Fenestrated, Size Ø7.5 mm | K2M Fenestrated Tap System | K2M, INC. |
| 29 | 10888857183124 | 5001-90015 | 5001-90015 | Tap, Fenestrated, Size Ø6.5 mm | K2M Fenestrated Tap System | K2M, INC. |
| 30 | 10888857183117 | 5001-90014 | 5001-90014 | Tap, Fenestrated, Size Ø5.5 mm | K2M Fenestrated Tap System | K2M, INC. |
| 31 | 10888857183100 | 5001-90013 | 5001-90013 | Tap, Fenestrated, Size Ø4.5 mm | K2M Fenestrated Tap System | K2M, INC. |
| 32 | 10888857183094 | 5001-90012 | 5001-90012 | Tap, Fenestrated, Size Ø4.0 mm | K2M Fenestrated Tap System | K2M, INC. |
| 33 | 10885403242021 | VBT1110 | VBT1110 | AVAMAX™ VERTEBRAL BALLOON TRAY 11GX10MM | AVAmax | CAREFUSION 2200, INC |
| 34 | 10885403241192 | AFB1130 | AFB1130 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX30MM | AVAflex | CAREFUSION 2200, INC |
| 35 | 10885403241185 | AFB1120 | AFB1120 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX20MM | AVAflex | CAREFUSION 2200, INC |
| 36 | 10885403241178 | AFB1115 | AFB1115 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX15MM | AVAflex | CAREFUSION 2200, INC |
| 37 | 10885403240911 | VBT1320 | VBT1320 | AVAMAX™ VERTEBRAL BALLOON TRAY 13GX20MM | AVAmax | CAREFUSION 2200, INC |
| 38 | 10885403240904 | VBT1315 | VBT1315 | AVAMAX™ VERTEBRAL BALLOON TRAY 13GX15MM | AVAmax | CAREFUSION 2200, INC |
| 39 | 10885403240898 | VBT1310 | VBT1310 | AVAMAX™ VERTEBRAL BALLOON TRAY 13GX10MM | AVAmax | CAREFUSION 2200, INC |
| 40 | 10885403225796 | AFB1030 | AFB1030 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 10GX20MM | AVAflex | CAREFUSION 2200, INC |
| 41 | 10885403223259 | AFB1015 | AFB1015 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 10GX15MM | AVAflex | CAREFUSION 2200, INC |
| 42 | 10885403223242 | AFB1020 | AFB1020 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 10GX20MM | AVAflex | CAREFUSION 2200, INC |
| 43 | 10885403219788 | AFH0010 | AFH0010 | AVAFLEX™ VERTEBRAL AUGMENTATION NEEDLE 10G | AVAflex | CAREFUSION 2200, INC |
| 44 | 10885403176593 | VBT1120 | VBT1120 | AVAMAX™ VERTEBRAL BALLOON TRAY 11GX20MM | AVAmax | CAREFUSION 2200, INC |
| 45 | 10885403176586 | VBT1115 | VBT1115 | AVAMAX™ VERTEBRAL BALLOON TRAY 11GX15MM | AVAmax | CAREFUSION 2200, INC |
| 46 | 10885403164996 | AFH0011 | AFH0011 | AVAFLEX™ VERTEBRAL AUGMENTATION NEEDLE 11G | AVAflex | CAREFUSION 2200, INC |
| 47 | 10885403120022 | VBT1015 | VBT1015 | AVAMAX™ VERTEBRAL BALLOON TRAY 10GX15MM | AVAmax | CAREFUSION 2200, INC |
| 48 | 10885403119996 | VBT1010 | VBT1010 | AVAMAX™ VERTEBRAL BALLOON TRAY 10GX10MM | AVAmax | CAREFUSION 2200, INC |
| 49 | 10885403119804 | VBT1020 | VBT1020 | AVAMAX™ VERTEBRAL BALLOON TRAY 10GX20MM | AVAmax | CAREFUSION 2200, INC |
| 50 | 10885403002120 | VMXXLCT | VMXXLCT | AVAmax PLUS Extra Level Tray Bone Cement Delivery System | AVAmax | CAREFUSION 2200, INC |