Other products from "OSSEON LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 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. NDN,HRX Cement, Bone, Vertebroplasty,Arthroscope 2 Osseoflex SB Straight Balloon (10ga/2ml)
2 B330OF03480 OF-0348 Osseoflex® CD-H Hydraulic Cement Delivery system is a bone cement delivery devic Osseoflex® CD-H Hydraulic Cement Delivery system is a bone cement delivery device designed to allow the physician to keep a safer distance from the radiation source during the cement delivery phase in vertebroplasty, vertebral augmentation procedures and the skeletal system. KIH Dispenser, Cement 1 Osseoflex CD-H
3 B330PC02700 PC-0270 The Osseoflex PC Pre-Curved Bone Tamp is a mechanical device used to disrupt can The Osseoflex PC Pre-Curved Bone Tamp is a mechanical device used to disrupt cancellous bone by channeling through the bone creating a void within a vertebral body. The Osseoflex PC Pre-Curved Bone Tamp can be utilized for multiple level vertebral body access. The channel can be used to introduce an appropriately sized Osseon inflatable bone tamp. HXG Tamp 1 Osseoflex PC Pre-Curved Bone Tamp 10ga
4 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. NDN,HRX Cement, Bone, Vertebroplasty,Arthroscope 2 Osseoflex SB Steerable Balloon (10ga/2ml)
5 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. NDN,HRX Cement, Bone, Vertebroplasty,Arthroscope 2 Osseoflex SB Straight Balloon (10ga/4ml)
6 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. NDN,HRX Cement, Bone, Vertebroplasty,Arthroscope 2 Osseoflex SB Steerable Balloon ( 10 ga/ 4ml)
7 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. NDN,HRX Cement, Bone, Vertebroplasty,Arthroscope 2 Osseoflex SB Steerable Balloon (8ga/ 4ml)
Other products with the same Product Codes "NDN, HRX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 04546540956958 4100600000 4100-600-000 1:1 Bur Attachment NA STRYKER CORPORATION
2 04546540905451 0407280000 0407280000 Percutaneous Discectomy Probe NA STRYKER CORPORATION
3 04546540905321 0407260000 0407260000 Percutaneous Discectomy Probe NA STRYKER CORPORATION
4 04546540905284 0407255000 0407255000 Cannula with Round Tip Stylet NA STRYKER CORPORATION
5 04546540616715 4100410000 4100-410-000 Radiolucent Adapter NA STRYKER CORPORATION
6 04546540616708 4100120000 4100-120-000 T-Latch Attachment NA STRYKER CORPORATION
7 04546540531827 0407251000 0407251000 Percutaneous Discectomy Probe with Curved Cannula NA STRYKER CORPORATION
8 04546540500229 0407281000 0407281000 Percutaneous Discectomy Probe NA STRYKER CORPORATION
9 04546540466266 0407254000 0407254000 Curved Cannula with Curved Bevel Tip Stylet NA STRYKER CORPORATION
10 04546540466259 0407253000 0407253000 Cannula with Bevel Tip Stylet NA STRYKER CORPORATION
11 04546540466242 0407250000 0407250000 Percutaneous Lumbar Discectomy Probe NA STRYKER CORPORATION
12 04546540434364 0406202000 0406-202-000 Radiopaque Bone Cement SpinePlex STRYKER CORPORATION
13 04546540401717 4100700000 4100-700-000 High Speed Bur Attachment NA STRYKER CORPORATION
14 04546540378101 4215000000 4215-000-000 Battery NA STRYKER CORPORATION
15 04546540378095 4212000000 4212-000-000 Battery NA STRYKER CORPORATION
16 04546540378002 4100134000 4100-134-000 Keyless Drill NA STRYKER CORPORATION
17 04546540377999 4100133000 4100-133-000 Keyless Drill NA STRYKER CORPORATION
18 04546540377982 4100126000 4100-126-000 Pin Collet NA STRYKER CORPORATION
19 04546540374165 4226120000 4226-120-000 CD2 Large Aseptic Housing NA STRYKER CORPORATION
20 04546540374141 4222120000 4222-120-000 Cordless Driver Small Aseptic Housing NA STRYKER CORPORATION
21 04546540374134 4222110000 4222-110-000 Non-Sterile Small Battery NA STRYKER CORPORATION
22 04546540371201 4222000000 4222-000-000 Cordless Driver Small Aseptic Battery Kit NA STRYKER CORPORATION
23 04546540134882 01-03731 01-03731 ADAPTER, ACMI/BRITISH STD FOR 01-03730 NA STRYKER LEIBINGER GMBH & CO. KG
24 04546540134875 01-03730 01-03730 SPARE FIBER-OPTIC CABLE NA STRYKER LEIBINGER GMBH & CO. KG
25 04546540068590 4112000000 4112-000-000 Battery Pack NA STRYKER CORPORATION
26 04546540068545 4110112000 4110-112-000 Battery Pack Adapter NA STRYKER CORPORATION
27 04546540068354 4100062000 4100-062-000 Wire Collet NA STRYKER CORPORATION
28 04546540068323 4100400000 4100-400-000 Sagittal Saw Attachment NA STRYKER CORPORATION
29 04546540068279 4100355000 4100-355-000 Radiolucent Right Angle Drive NA STRYKER CORPORATION
30 04546540068262 4100335000 4100-335-000 Right Angle Drive - Modified Trinkle Reamer NA STRYKER CORPORATION
31 04546540068248 4100260000 4100-260-000 Trinkle Reamer NA STRYKER CORPORATION
32 04546540068231 4100235000 4100-235-000 Modified Trinkle Reamer Hudson STRYKER CORPORATION
33 04546540068224 4100231000 4100-231-000 Reamer NA STRYKER CORPORATION
34 04546540068217 4100210000 4100-210-000 Large Reamer AO STRYKER CORPORATION
35 04546540068200 4100160000 4100-160-000 Trinkle Drill NA STRYKER CORPORATION
36 04546540068194 4100135000 4100-135-000 Modified Trinkle Drill Hudson STRYKER CORPORATION
37 04546540068187 4100132000 4100-132-000 Drill NA STRYKER CORPORATION
38 04546540068170 4100131000 4100-131-000 Keyed Chuck NA STRYKER CORPORATION
39 04546540068156 4100110000 4100-110-000 Small Drill AO STRYKER CORPORATION
40 04260200314109 1002-TS 010 TOM Endo Stick MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
41 04260200314093 1002-TS 009 TOM Endo Stick MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
42 04260200314086 1002-TS 008 TOM Endo Stick MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
43 04260200314079 1002-TS 007 TOM Endo Stick MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
44 04260200311832 1002-TS 005 TOM Endo Stick 2,1 mm short MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
45 04260200311795 1002-TS 002 TOM Endo Stick 2,1 mm MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
46 04260200311153 1002-TS 003 TOM Endo Stick 4,1 mm MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
47 04260200311146 1002-TS 001 TOM Endo Stick 3,7 mm MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
48 04260200311139 1002-TS 004 TOM Endo Stick MaxMoreSpine HOOGLAND SPINE PRODUCTS GMBH
49 04260102132597 plus 66045747 OSTEOPAL® plus is a radiopaque, low-viscosity bonecement, based on polymethyl me OSTEOPAL® plus is a radiopaque, low-viscosity bonecement, based on polymethyl methacrylate with anextended application phase, used to fill and stabilize vertebral bodies. OSTEOPAL® plus contains zirconium dioxide as an X-ray contrast agent. OSTEOPAL® plus contains the coloring agent chlorophyll VIII (E141) to improve visibility in the surgical field. The bone cement is prepared immediately prior to use by mixing the polymer powder component and the liquid monomer component. A low viscosity paste is applied with the use of application system, placed in the vertebral body, where it cures. OSTEOPAL® plus conforms to ISO 5833 except Annex C OSTEOPAL® HERAEUS MEDICAL GMBH
50 04260102130494 V 66031896 Osteopal® V is an acrylic cement for use in vertebroplasty and kyphoplasty. It i Osteopal® V is an acrylic cement for use in vertebroplasty and kyphoplasty. It is formed from powder and liquid by exothermic polymerization OSTEOPAL® HERAEUS MEDICAL GMBH