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.
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.
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.
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.
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.
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.
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.
RALLY ALL IN ONE CEMENT GUN is intended to be used for helping the extrusion (an
RALLY ALL IN ONE CEMENT GUN is intended to be used for helping the extrusion (and hence the delivery) of the bone cement prepared with the RALLY ALL IN ONE SYSTEM devices.
GUN-01 is intended to be used for helping the extrusion (and hence the delivery)
GUN-01 is intended to be used for helping the extrusion (and hence the delivery) of bone cement only from the Tecres’ syringes Cemex System Device.
BONE INJECTION NEEDLE beveled tip 13 Gauge 120 mm length with metal handgrip int
BONE INJECTION NEEDLE beveled tip 13 Gauge 120 mm length with metal handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 13 Gauge 120 mm length
BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with plastic handgrip i
BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length
BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with plastic handgrip i
BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length
BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with metal handgrip int
BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with metal handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length
BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with metal handgrip int
BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with metal handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length
BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with metal handgrip inte
BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with metal handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length
BONE INJECTION NEEDLE beveled tip 13 Gauge 120 mm length with plastic handgrip i
BONE INJECTION NEEDLE beveled tip 13 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 13 Gauge 120 mm length
BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with plastic handgrip in
BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length
BONE INJECTION NEEDLE diamond tip 15 Gauge 120 mm length with plastic handgrip i
BONE INJECTION NEEDLE diamond tip 15 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE diamond tip 15 Gauge 120 mm length
BONE INJECTION NEEDLE diamond tip 13 Gauge 120 mm length with plastic handgrip i
BONE INJECTION NEEDLE diamond tip 13 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE diamond tip 13 Gauge 120 mm length
BONE INJECTION NEEDLE diamond tip 11 Gauge 120 mm length with plastic handgrip i
BONE INJECTION NEEDLE diamond tip 11 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE diamond tip 11 Gauge 120 mm length
BONE INJECTION NEEDLE diamond tip 9 Gauge 150 mm length with plastic handgrip in
BONE INJECTION NEEDLE diamond tip 9 Gauge 150 mm length with plastic handgrip intended for the injection of acrylic resin.
BONE INJECTION NEEDLE diamond tip 9 Gauge 150 mm length
The icotec cement cannula is a sterile packed cannula designed for the augmentat
The icotec cement cannula is a sterile packed cannula designed for the augmentation with icotec implants.
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ Sys
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ System, is a sterile packed kit for Vertebroplasty procedures. The needle kit is to be used in conjunction with PMMA cement and appropriate syringes.
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ Sys
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ System, is a sterile packed kit for Vertebroplasty procedures. The needle kit is to be used in conjunction with PMMA cement and appropriate syringes.
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ Sys
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ System, is a sterile packed kit for Vertebroplasty procedures. The needle kit is to be used in conjunction with PMMA cement and appropriate syringes.
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ Sys
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ System, is a sterile packed kit for Vertebroplasty procedures. The needle kit is to be used in conjunction with PMMA cement and appropriate syringes.
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ Sys
The “Vertebroplasty Needle Kit“, part of the Synthes’ Vertecem / Vertecem V+ System, is a sterile packed kit for Vertebroplasty procedures. The needle kit is to be used in conjunction with PMMA cement and appropriate syringes.
The PALACOS® MV+G pro system consists of a mixing and application system prefill
The PALACOS® MV+G pro system consists of a mixing and application system prefilled with PALACOS® polymer powder and monomer liquid. PALACOS® MV+G pro is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.