Other products from "SINTEA PLUSTEK SRL"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 08057432561366 PLS-5070T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
2 08057432561342 SPS-27S550 NDN,HXG Cement, Bone, Vertebroplasty,Tamp 1 SPIDER KOLIBRI
3 08057432561304    PLS-555T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
4 08057432561144 PLS-740T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
5 08057432561120 PLS-730T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
6 08057432561090 PLS-745T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
7 08057432560918    PLS-540T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
8 08057432560895    PLS-530T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
9 08057432560864 LFC-002PK3209 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF LITE
10 08057432560857 LFC-002PK3207 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF LITE
11 08057432560680    PLS-1095T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
12 08057432560666 SPS-26S645 NDN,HXG Cement, Bone, Vertebroplasty,Tamp 1 SPIDER KOLIBRI
13 08057432560628 SPS-26S540 NDN,HXG Cement, Bone, Vertebroplasty,Tamp 1 SPIDER KOLIBRI
14 08057432564114 PLS-840T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
15 08057432564077 PLS-5095T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
16 08057432564060 PLS-5090T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
17 08057432564053 PLS-5085T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
18 08057432564039 PLS-5075T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
19 08057432563995 PLS-5095T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
20 08057432563964 PLS-5080T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
21 08057432563933 PLS-5065T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
22 08057432563926 PLS-5100T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
23 08057432564497 PLS-8080T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
24 08057432564480 PLS-875T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
25 08057432564473 PLS-870T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
26 08057432563889 PLS-5080T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
27 08057432563858 PLS-5065T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
28 08057432563810 PLS-1085T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
29 08057432563803 PLS-1080T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
30 08057432563797 PLS-1075T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
31 08057432563711 PLS-10080T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
32 08057432563698 PLS-10070T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
33 08057432563629 PLS-10035T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
34 08057432563612 PLS-10030T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
35 08057432563599 PLS-10095T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
36 08057432563520 PLS-10060T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
37 08057432563513 PLS-10055T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
38 08057432563490 PLS-10045T57 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
39 08057432563360 PLS-10055T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
40 08057432563353 PLS-10050T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
41 08057432563308 PLS-10100T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
42 08057432563285 PLS-10090T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
43 08057432563247 PLS-10070T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
44 08057432563223 PLS-10060T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
45 08057432563216 PLS-10055T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
46 08057432563179 PLS-10035T55 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
47 08057432563131 PLS-10090T540 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
48 08057432562967   PLS-61T56 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
49 08057432562912 PLS-960T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
50 08057432562899 PLS-950T58 KWP Appliance, Fixation, Spinal Interlaminal 2 PLS
Other products with the same Product Codes "HXG, NDN"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00190776059439 VM88-1038 Bone Tamper Avalign AVALIGN TECHNOLOGIES, INC.
2 00190660217136 Bone tamper 45-398 Bone tamper, 6'', 9.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
3 00190660210960 Bone tamper 45-442 Bone tamper, 8'', 16.0mm diameter, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
4 00190660210953 Bone tamper 45-441 Bone tamper, 8'', 14.0mm diameter, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
5 00190660210946 Bone tamper 45-440 Bone tamper, 8'', 12.0mm diameter, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
6 00190660195649 Sypert bone tamper 45-418 Sypert bone tamper, 11 1/2'', 6.0mm x 20.0mm, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
7 00190660195632 Sypert bone tamper 45-417 Sypert bone tamper, 11 1/2'', 5.0mm x 15.0mm, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
8 00190660195625 Sypert bone tamper 45-416 Sypert bone tamper, 11 1/2'', 4.0mm x 10.0mm, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
9 00190660195618 Sypert bone tamper 45-415 Sypert bone tamper, 11 1/2'', 3.0mm x 8.0mm, round/flat handle Ambler Surgical AMBLER SURGICAL CORP.
10 00190660111748 Bone tamper 45-396 Bone tamper, 6'', 8.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
11 00190660111731 Bone tamper 45-395 Bone tamper, 6'', 7.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
12 00190660111724 Bone tamper 45-394 Bone tamper, 6'', 6.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
13 00190660111717 Bone tamper 45-393 Bone tamper, 6'', 5.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
14 00190660111700 Bone tamper 45-392 Bone tamper, 6'', 4.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
15 00190660111694 Bone tamper 45-391 Bone tamper, 6'', 3.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
16 00190660111687 Bone tamper 45-390 Bone tamper, 6'', 2.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
17 00190660111670 Bone tamper 45-397 Bone tamper, 6'', 10.0mm diameter, round handle Ambler Surgical AMBLER SURGICAL CORP.
18 00190660082819 Small quick coupling t-handle 43-056 Small quick coupling t-handle, 3 1/2'' Ambler Surgical AMBLER SURGICAL CORP.
19 00190376367125 233-950 IdentiTi ALIF SA, Tamp, Offset IdentiTi ALPHATEC SPINE, INC.
20 00190376364902 233-900 IdentiTi ALIF SA, Tamp, Straight, Footed IdentiTi ALPHATEC SPINE, INC.
21 00190376355795 321-500-20 PSX Lordotic Expandable, Graft Tamp PSX ALPHATEC SPINE, INC.
22 00190376284828 133-900 IDENTITi ALIF SA, TAMP, STRAIGHT, FOOTED IdentiTi ALPHATEC SPINE, INC.
23 00190376274904 135-800 CERVICAL INTERFIXATED TAMP IdentiTi ALPHATEC SPINE, INC.
24 00190376213835 125-600 Graft Tamp IdentiTi ALPHATEC SPINE, INC.
25 00190376213828 125-310 Tamp, Straight IdentiTi ALPHATEC SPINE, INC.
26 00190376213811 125-300 PO Tamp, Forked IdentiTi ALPHATEC SPINE, INC.
27 00190376204604 130-310 ALIF Straight Tamp, Single-Prong IdentiTi ALPHATEC SPINE, INC.
28 00190376204598 130-300 ALIF Straight Tamp, Dual-Prong IdentiTi ALPHATEC SPINE, INC.
29 00190376180311 121-300 PS TAMP, FORKED IdentiTi ALPHATEC SPINE, INC.
30 00190376174358 123-320 TAMP, STRAIGHT IdentiTi ALPHATEC SPINE, INC.
31 00190376174341 123-310 IMPLANT POSITIONER, ANGLED IdentiTi ALPHATEC SPINE, INC.
32 00190376174334 123-300 IMPLANT POSITIONER, STRAIGHT IdentiTi ALPHATEC SPINE, INC.
33 00190376172507 127-401 CERVICAL GRAFT PACKING TAMP IdentiTi ALPHATEC SPINE, INC.
34 00190376172484 127-300 CERVICAL TAMP IdentiTi ALPHATEC SPINE, INC.
35 00190376151168 94337-310 PO INST, STRAIGHT TAMP, SHORT IdentiTi ALPHATEC SPINE, INC.
36 00190376151144 94337-300 PO INST, STRAIGHT TAMP, LONG IdentiTi ALPHATEC SPINE, INC.
37 00190376148748 114-310 ALIF INST, STRAIGHT TAMP, SINGLE-PRONG IdentiTi ALPHATEC SPINE, INC.
38 00190376148731 114-300 ALIF INST, STRAIGHT TAMP, DUAL-PRONG IdentiTi ALPHATEC SPINE, INC.
39 B471240000020 24000002 Staple Tamp, Large GEO Staple System GRAMERCY EXTREMITY ORTHOPEDICS LLC
40 B471240000010 24000001 Staple Tamp, Small GEO Staple System GRAMERCY EXTREMITY ORTHOPEDICS LLC
41 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. Osseoflex PC Pre-Curved Bone Tamp 10ga OSSEON LLC
42 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
43 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
44 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
45 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
46 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
47 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
48 B07330K0160400 30-K01-6040 30-K01-6040 Tamp, Angled Navagio KALITEC DIRECT LLC
49 B07330K0160300 30-K01-6030 30-K01-6030 Tamp, Footed Navagio KALITEC DIRECT LLC
50 B07330K0160200 30-K01-6020 30-K01-6020 Tamp, Straight Navagio KALITEC DIRECT LLC