No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00842166187627 | ZAV-1194-S-11 | Paddle Shaver 11 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
2 | 00842166187603 | ZAV-1194-S-09 | Paddle Shaver 09 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
3 | 00842166187597 | ZAV-1194-S-08 | Paddle Shaver 08 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
4 | 00842166187634 | ZAV-1194-S-12 | Paddle Shaver 12 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
5 | 00842166188754 | ZAV-1228-5 | 5mm Dilator | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
6 | 00842166187948 | ZAV-1205 | Custom Graft Pusher | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Zavation | |
7 | 00842166187665 | ZAV-1194-S-15 | Paddle Shaver 15 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
8 | 00842166187658 | ZAV-1194-S-14 | Paddle Shaver 14 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
9 | 00842166187641 | ZAV-1194-S-13 | Paddle Shaver 13 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
10 | 00842166187610 | ZAV-1194-S-10 | Paddle Shaver 10 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
11 | 00842166187580 | ZAV-1194-S-07 | Paddle Shaver 07 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
12 | 00842166187245 | ZAV-1182-S15 | Paddle Shaver 15 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
13 | 00842166187238 | ZAV-1182-S14 | Paddle Shaver 14 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
14 | 00842166187221 | ZAV-1182-S13 | Paddle Shaver 13 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
15 | 00842166187214 | ZAV-1182-S12 | Paddle Shaver 12 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
16 | 00842166187207 | ZAV-1182-S11 | Paddle Shaver 11 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
17 | 00842166187191 | ZAV-1182-S10 | Paddle Shaver 10 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
18 | 00842166187184 | ZAV-1182-S09 | Paddle Shaver 09 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
19 | 00842166187177 | ZAV-1182-S08 | Paddle Shaver 08 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
20 | 00842166187160 | ZAV-1182-S07 | Paddle Shaver 07 | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
21 | 00842166185258 | 410-1059 | Torque Limiting Handle | NKB,KWQ | Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Intervertebral Body | 2 | Zavation | |
22 | 00842166185241 | 410-1058-50 | Drill 5.0 | KWQ,NKB | Appliance, Fixation, Spinal Intervertebral Body,Thoracolumbosacral Pedicle Screw System | 2 | Zavation | |
23 | 00842166185234 | 410-1058-40 | Drill 4.0 | NKB,KWQ | Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Intervertebral Body | 2 | Zavation | |
24 | 00842166185227 | 410-1058-35 | Drill 3.5 | KWQ,NKB | Appliance, Fixation, Spinal Intervertebral Body,Thoracolumbosacral Pedicle Screw System | 2 | Zavation | |
25 | 00842166185210 | 410-1058-30 | Drill 3.0 | NKB,KWQ | Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Intervertebral Body | 2 | Zavation | |
26 | 00842166185203 | 410-1056 | Adjustable Drill Guide | KWQ,NKB | Appliance, Fixation, Spinal Intervertebral Body,Thoracolumbosacral Pedicle Screw System | 2 | Zavation | |
27 | 00842166185197 | 410-1005-50 | Tap | NKB,KWQ | Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Intervertebral Body | 2 | Zavation | |
28 | 00842166185180 | Z-1031 | Fixed, Palm, A-O, Pull | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
29 | 00842166185173 | ZAV-1153 | Custom Persuader | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
30 | 00842166183360 | ZAV-1141 | Lumbar Rod Builder | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
31 | 00842166181717 | ZAV-1115-13 | 13mm Dilator | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
32 | 00842166181700 | ZAV-1115-9 | 9mm Dilator | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Zavation | |
33 | 00842166181694 | ZAV-1115-5 | 5mm Dilator | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
34 | 00842166181687 | ZAV-1114 | Straight Tamp | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Zavation | |
35 | 00842166181670 | ZAV-1113-14 | Custom Peek Dilator | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
36 | 00842166180857 | ZAV-1098-75 | 7.5mm Tapered Tap | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Zavation | |
37 | 00842166180840 | ZAV-1098-65 | 6.5mm Tapered Tap | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
38 | 00842166180833 | ZAV-1098-55 | 5.5mm Tapered Tap | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Zavation | |
39 | 00842166180826 | ZAV-1097 | Custom Awl | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Zavation | |
40 | 00842166180819 | ZAV-1096 | Custom Universal Driver | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
41 | 00842166195080 | 30-9013 | 1-2 Level Cervical Plate Tray | KWQ | Appliance, Fixation, Spinal Intervertebral Body | 2 | Zavation | |
42 | 00842166180802 | ZAV-1093 | Custom Driver Sleeve | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Zavation | |
43 | 00842166180796 | ZAV-1098 | 7.5mm Tapered Tap | MNI,MNH,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | Zavation | |
44 | 00842166180789 | 290-1014 | Removal Drill | MRW | System, Facet Screw Spinal Device | U | Zavation | |
45 | 00842166180772 | 290-1013 | Bone Graft Tamp | MRW | System, Facet Screw Spinal Device | U | Zavation | |
46 | 00842166195073 | 210-9000 | Z-Direct Instrument Tray | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Zavation | |
47 | 00842166180765 | 290-1012 | Bone Graft Funnel | MRW | System, Facet Screw Spinal Device | U | Zavation | |
48 | 00842166180758 | 290-1011 | Screw Driver | MRW | System, Facet Screw Spinal Device | U | Zavation | |
49 | 00842166195066 | 259-9000 | Normandy VBR System Tray | MQP,PLR | Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical | 2 | Zavation | |
50 | 00842166195240 | 0100004 5487-400-001 | Primary Instrument Case 6 deg - Assembly | OVD,MAX | Intervertebral Fusion Device With Integrated Fixation, Lumbar,Intervertebral Fus Intervertebral Fusion Device With Integrated Fixation, Lumbar,Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Zavation |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | B39034191 | 3419 | Reprocessed 2.9mm Full Radius Blade | SURETEK MEDICAL | ||
2 | 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 | |
3 | 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 | |
4 | 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 | |
5 | 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 | |
6 | 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 | |
7 | 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 | |
8 | 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 | |
9 | 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 | |
10 | 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 | |
11 | 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 | |
12 | 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 | |
13 | 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 | |
14 | B235MDK00010 | MDK-0001 | MDK-0001 | mild Device Kit | VERTOS MEDICAL, INC. | |
15 | B21232341 | 32-34 | 32-34 | 16 Gauge x 3.5" Aspirating Needle, W/ Blunt Cannula. Sterile, Individually Blist 16 Gauge x 3.5" Aspirating Needle, W/ Blunt Cannula. Sterile, Individually Blister Packed, Box of 100 | Aspirating Needle | INTERNATIONAL MEDICAL INDUSTRIES INC. |
16 | B21232321 | 32-32 | 32-32 | 16 Gauge x 8" Aspirating Needle, W/ Blunt Cannula. Sterile & Non-Pyrogenic, Indi 16 Gauge x 8" Aspirating Needle, W/ Blunt Cannula. Sterile & Non-Pyrogenic, Individually Blister Packed, Box of 100 | Aspirating Needle | INTERNATIONAL MEDICAL INDUSTRIES INC. |
17 | B21232311 | 32-31 | 32-31 | 16 Gauge x 5" Aspirating Needle, W/ Blunt Cannula. Sterile & Non-Pyrogenic, Indi 16 Gauge x 5" Aspirating Needle, W/ Blunt Cannula. Sterile & Non-Pyrogenic, Individually Blister Packed, Box of 100 | Aspirating Needle | INTERNATIONAL MEDICAL INDUSTRIES INC. |
18 | B21232231 | 32-23 | 32-23 | 19 Gauge x 8" Aspirating Needle, W/ Sharp Cannula. Sterile & Non-Pyrogenic, Indi 19 Gauge x 8" Aspirating Needle, W/ Sharp Cannula. Sterile & Non-Pyrogenic, Individually Blister Packed, Box of 100 | Aspirating Needle | INTERNATIONAL MEDICAL INDUSTRIES INC. |
19 | B21232221 | 32-22 | 32-22 | 19 Gauge x 5" Aspirating Needle, W/ Sharp Cannula. Sterile & Non-Pyrogenic, Indi 19 Gauge x 5" Aspirating Needle, W/ Sharp Cannula. Sterile & Non-Pyrogenic, Individually Blister Packed, Box of 100 | Aspirating Needle | INTERNATIONAL MEDICAL INDUSTRIES INC. |
20 | B21232211 | 32-21 | 32-21 | 19 Gauge x 3" Aspirating Needle, W/ Sharp Cannula. Sterile & Non-Pyrogenic, Indi 19 Gauge x 3" Aspirating Needle, W/ Sharp Cannula. Sterile & Non-Pyrogenic, Individually Blister Packed, Box of 100 | Aspirating Needle | INTERNATIONAL MEDICAL INDUSTRIES INC. |
21 | B192300311000 | 30-0311-00 | 30-0311-00 | 4.0 mm, 45 deg. Sinuscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
22 | B192300012000 | 30-0012-00 | 30-0012-00 | 4.0 mm, 70 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
23 | B192300011000 | 30-0011-00 | 30-0011-00 | 4.0 mm, 30 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
24 | B192300010000 | 30-0010-00 | 30-0010-00 | 4.0 mm, 0 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
25 | B192300008000 | 30-0008-00 | 30-0008-00 | 2.7 mm, 30 deg. Arthroscope, l=187.5mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
26 | B192300006000 | 30-0006-00 | 30-0006-00 | 2.7 mm, 70 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
27 | B192300004000 | 30-0004-00 | 30-0004-00 | 2.7 mm, 0 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
28 | B192300003000 | 30-0003-00 | 30-0003-00 | 2.7 mm, 70 deg. Arthroscope, l=110mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
29 | B169DBNS30100 | DBNS-30-10 | DBNS-30-10 | Short Disposable Biopsy Needle w/Removable Depth Stop | Compass International | COMPASS INTERNATIONAL |
30 | B169DBNPS3010T0 | DBNPS-30-10T | DBNPS-30-10T | Short Disposable 10mm Biopsy Needle w/Movable Depth Stop & Tracker | Compass International | COMPASS INTERNATIONAL |
31 | B169DBNP3010S0 | DBNP-30-10S | DBNP-30-10S | Long Disposable Biopsy Needle w/Fixed Stainless Steel Depth Stop | Compass International | COMPASS INTERNATIONAL |
32 | B169DBNP1010TP0 | DBNP-10-10TP | DBNP-10-10TP | Cygnus-PFS TracPlus Disposable Biopsy Needle | Compass International | COMPASS INTERNATIONAL |
33 | B169DBN30100 | DBN-30-10 | DBN-30-10 | Disposable Biopsy Needle Removable Depth Stop | Compass International | COMPASS INTERNATIONAL |
34 | B089B659660 | B65966 | B65966 | ENDOPLASTIC SCOPE; 12''(33CM, )30 DEGREE, 10MM DIAMETER, | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
35 | B089B659320 | B65932 | B65932 | SINUSCOPE OBTURATOR CONICAL BLUNT, 3.0 MM, 140 LENGTH | N/A | BLACK & BLACK SURGICAL, INC. |
36 | B089B659310 | B65931 | B65931 | SINUSCOPE TROCAR WITH PYRAMIDAL TIP, 3.0 MM, 140 LENGTH | N/A | BLACK & BLACK SURGICAL, INC. |
37 | B089B659300 | B65930 | B65930 | SINUSCOPE TROCAR SLEEVE, UNIVERSAL, FOR 3.0 MM SCOPES, 140 LENGTH, "0"d, "30"d, "70"d | N/A | BLACK & BLACK SURGICAL, INC. |
38 | B089B659250 | B65925 | B65925 | ENDOPLASTIC SCOPE; 12''(33CM), 0 DEGREE, 10MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
39 | B089B659220 | B65922 | B65922 | ENDOPLASTIC SCOPE; 7"(18CM), 0 DEGREE, 4MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
40 | B089B659210 | B65921 | B65921 | ENDOPLASTIC SCOPE; 7''(17.5CM), 30 DEGREE, 4MM DIAMETER, | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
41 | B089B659200 | B65920 | B65920 | ENDOPLASTIC SCOPE; 7"(17.5CM), 30 DEGREE, 5MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
42 | B089B659100 | B65910 | B65910 | ENDOPLASTIC SCOPE; 7''(17.5CM), 30 DEGREE, 10MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
43 | B089B659050 | B65905 | B65905 | OTOSCOPE; 1.6''(41MM), 0 DEGREE, 2.7MM DIAMETER, AUTOCLAVABLE | N/A | BLACK & BLACK SURGICAL, INC. |
44 | B089B659010 | B65901 | B65901 | SINUSCOPE; 5 3/4"(14.0CM), "30" DEGREE, 3.0MM DIAMETER, AUTOCLAVABLE | N/A | BLACK & BLACK SURGICAL, INC. |
45 | B089B659000 | B65900 | B65900 | SINUSCOPE; 5 3/4"(14.0CM), "0" DEGREE, 3.0MM DIAMETER, AUTOCLAVABLE | N/A | BLACK & BLACK SURGICAL, INC. |
46 | B067212001 | 21200 | 21200 | 2.0 MM Short Kit with aspiration bottle | Nucleotome | CLARUS MEDICAL, LLC |
47 | 88719214221665 | CN27.D05 | 27G Blunt Needles with luer-lock connector | VitreQ | VITREQ B.V. | |
48 | 88719214221641 | CN25.D05 | 25G Blunt Needles with luer-lock connector | VitreQ | VITREQ B.V. | |
49 | 88719214221627 | CN23.D05 | 23G Blunt Needles with luer-lock connector | VitreQ | VITREQ B.V. | |
50 | 88719214221603 | CN25.D04 | 25G Pick Needles | VitreQ | VITREQ B.V. |