BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
Integra™ Ventricular Drainage System provides a sterile path for the drainage of
Integra™ Ventricular Drainage System provides a sterile path for the drainage of cerebrospinal fluid (CSF) from an intraventricular catheter to a collection bag. The system can be used for external drainage, and the management of hydrocephalic shunt infections, or treatment of other cerebral conditions such as pre-operative or post-operative pressure monitoring of CSF to control increased intracranial pressure.
Trel-X™Gel, 10cc is human bone that has been demineralized and combined with po
Trel-X™Gel, 10cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package.
Trel-XPress 100, 5cc is made using demineralized human bone mixed with poloxamer
Trel-XPress 100, 5cc is made using demineralized human bone mixed with poloxamer reverse phase medium. Trel-XPress 100 is formulated into a putty form and is provided in a sterile, single use package.
MQV,MBP
FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human
FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human growth factor)
Trel-XPress 100, 2.5cc is made using demineralized human bone mixed with poloxam
Trel-XPress 100, 2.5cc is made using demineralized human bone mixed with poloxamer reverse phase medium. Trel-XPress 100 is formulated into a putty form and is provided in a sterile, single use package.
MQV,MBP
FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human
FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human growth factor)
Trel-XPress 100, 10cc is made using demineralized human bone mixed with poloxame
Trel-XPress 100, 10cc is made using demineralized human bone mixed with poloxamer reverse phase medium. Trel-XPress 100 is formulated into a putty form and is provided in a sterile, single use package.
MQV,MBP
FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human
FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human growth factor)
Trel-X™Gel, 5cc is human bone that has been demineralized and combined with pol
Trel-X™Gel, 5cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package.
Trel-X™Gel, 1cc is human bone that has been demineralized and combined with pol
Trel-X™Gel, 1cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package.
The Evolution Pole Mount Assembly provides support and alignment for the Externa
The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket.
The Evolution Pole Mount Assembly provides support and alignment for the Externa
The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket.
The Evolution Pole Mount Assembly provides support and alignment for the Externa
The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket.
The Pole Mount Laser Level device is provided with mounting bracket for use with
The Pole Mount Laser Level device is provided with mounting bracket for use with Integra Pole Mount Assemblies. The Pole Mount Laser provides alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular catheter or lumbar catheter to an external ventricular drainage system.
The Evolution Pole Mount Assembly provides support and alignment for the Externa
The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket.
The Evolution Pole Mount Assembly provides support and alignment for the Externa
The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket.
The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of C
The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of CSF in children with small veins. The distal section of the catheter is reduced to approximately one-half standard diameter for easier insertion. The proximal section of the catheter contains an imbedded barium sulfate-impregnated strip, and the distal section is fully barium sulfate-impregnated. The infant model does not contain graduation markets.
The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of C
The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of CSF in children with small veins. The distal section of the catheter is reduced to approximately one-half standard diameter for easier insertion. The proximal section of the catheter contains an imbedded barium sulfate-impregnated strip, and the distal section is fully barium sulfate-impregnated. The infant model does not contain graduation markets.
NEURAWRAP 7MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable coll
NEURAWRAP 7MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve.
The External CSF Drainage Systems provide a sterile fluid path resistant to micr
The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. The systems are used to drain CSF from ventricles of the brain or the lumbar subarachnoid space to a drainage bag. System components facilitate CSF drainage, fluid injection, CSF sampling and intracranial pressure monitoring.
The External CSF Drainage Systems provide a sterile fluid path resistant to micr
The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. The systems are used to drain CSF from ventricles of the brain or the lumbar subarachnoid space to a drainage bag. System components facilitate CSF drainage, fluid injection, CSF sampling and intracranial pressure monitoring.
The Allegheny EVD System provides a sterile fluid path for the drainage of CSF f
The Allegheny EVD System provides a sterile fluid path for the drainage of CSF from an intraventricular catheter to a drainage bag. System components facilitate ventricular drainage, fluid injection, CSF sampling and intracranial pressure monitoring.
LIMITORR 30 MLVolume Limiting External CSF Drainage System with 20ml Burette.Lim
LIMITORR 30 MLVolume Limiting External CSF Drainage System with 20ml Burette.LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of cerebrospinal fluid (CSF) from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage System was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSFdrainage. The burette in the Volume Limiting External CSF Drainage System contains a volume limiting valve which stops drainage when the pre-determined volume (20ml or 30ml) is reached.
The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provide
The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of CSF from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage system was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSF drainage. The burette contains a volume limiting valve which stops drainage when the pre-determine volume (20ml or 30ml) is reached.
The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provide
The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of CSF from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage system was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSF drainage. The burette contains a volume limiting valve which stops drainage when the pre-determine volume (20ml or 30ml) is reached.
LIMITORR 20 MLVolume Limiting External CSF Drainage System with 20ml Burette.Lim
LIMITORR 20 MLVolume Limiting External CSF Drainage System with 20ml Burette.LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of cerebrospinal fluid (CSF) from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage System was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSFdrainage. The burette in the Volume Limiting External CSF Drainage System contains a volume limiting valve which stops drainage when the pre-determined volume (20ml or 30ml) is reached.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
NEURAWRAP 7MM 4CM NERVE PROTECTOR The NeuraWrap Nerve Protector is an absorbable
NEURAWRAP 7MM 4CM NERVE PROTECTOR The NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap Nerve Protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap Nerve Protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap Nerve Protector to recover and maintain closure once the device is placed around the nerve.
NEURAWRAP 5MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbab
NEURAWRAP 5MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve.
NEURAWRAP 5MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable coll
NEURAWRAP 5MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve.
NEURAWRAP 3MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbabl
NEURAWRAP 3MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve.
NEURAWRAP 3MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable coll
NEURAWRAP 3MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve.
NEURAWRAP 10MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbab
NEURAWRAP 10MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve.
The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of C
The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of CSF in children with small veins. The distal section of the catheter is reduced to approximately one-half standard diameter for easier insertion. The proximal section of the catheter contains an imbedded barium sulfate-impregnated strip, and the distal section is fully barium sulfate-impregnated. The infant model does not contain graduation markets.
Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for
Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for use in the reconstruction of soft tissue deficiencies.
Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for
Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for use in the reconstruction of soft tissue deficiencies.
TRAUMACATH VENTRICULAR CATHETER SETThe TraumaCath Ventricular Catheter set cathe
TRAUMACATH VENTRICULAR CATHETER SETThe TraumaCath Ventricular Catheter set catheter is barium striped. Designed for diverting fluid from the ventricles through a series of drainage holes, the catheter can be inserted into the ventricular cavity with the stainless steel stylet. A trocar is supplied with the catheter to facilitate subcutaneous tunneling away from the burr hole. The external portion of the catheter may be secured to the scalp by the suture tab. The luer lock supplied with each ventricular catheter set will connect the catheter to any Integra external drainage system.
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one open end, one sealed end (cap) and internal channels designed to provide protection for a peripheral nerve end or stump where repair is unattainable or not desired. The device isolates the nerve stump from the surrounding soft tissue bed by pulling the nerve into the tube and suturing the nerve within the cap. The end of the cap has a suturable tab to allow the surgeon to suture the device to surrounding tissue. AxoGuard® Nerve Cap is an extracellular matrix (ECM) and is fully remodeled during the healing process. When hydrated, AxoGuard® Nerve Cap is easy to handle, soft, pliable, nonfriable and porous. AxoGuard® Nerve Cap is flexible and pliable to accommodate movement of the joints and surrounding soft tissues and has sufficient mechanical strength to hold appropriately sized non-absorbable suture. AxoGuard® Nerve Cap is provided sterile, for single use only, and in a variety of sizes to meet clinical needs.
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one open end, one sealed end (cap) and internal channels designed to provide protection for a peripheral nerve end or stump where repair is unattainable or not desired. The device isolates the nerve stump from the surrounding soft tissue bed by pulling the nerve into the tube and suturing the nerve within the cap. The end of the cap has a suturable tab to allow the surgeon to suture the device to surrounding tissue. AxoGuard® Nerve Cap is an extracellular matrix (ECM) and is fully remodeled during the healing process. When hydrated, AxoGuard® Nerve Cap is easy to handle, soft, pliable, nonfriable and porous. AxoGuard® Nerve Cap is flexible and pliable to accommodate movement of the joints and surrounding soft tissues and has sufficient mechanical strength to hold appropriately sized non-absorbable suture. AxoGuard® Nerve Cap is provided sterile, for single use only, and in a variety of sizes to meet clinical needs.
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one open end, one sealed end (cap) and internal channels designed to provide protection for a peripheral nerve end or stump where repair is unattainable or not desired. The device isolates the nerve stump from the surrounding soft tissue bed by pulling the nerve into the tube and suturing the nerve within the cap. The end of the cap has a suturable tab to allow the surgeon to suture the device to surrounding tissue. AxoGuard® Nerve Cap is an extracellular matrix (ECM) and is fully remodeled during the healing process. When hydrated, AxoGuard® Nerve Cap is easy to handle, soft, pliable, nonfriable and porous. AxoGuard® Nerve Cap is flexible and pliable to accommodate movement of the joints and surrounding soft tissues and has sufficient mechanical strength to hold appropriately sized non-absorbable suture. AxoGuard® Nerve Cap is provided sterile, for single use only, and in a variety of sizes to meet clinical needs.
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one open end, one sealed end (cap) and internal channels designed to provide protection for a peripheral nerve end or stump where repair is unattainable or not desired. The device isolates the nerve stump from the surrounding soft tissue bed by pulling the nerve into the tube and suturing the nerve within the cap. The end of the cap has a suturable tab to allow the surgeon to suture the device to surrounding tissue. AxoGuard® Nerve Cap is an extracellular matrix (ECM) and is fully remodeled during the healing process. When hydrated, AxoGuard® Nerve Cap is easy to handle, soft, pliable, nonfriable and porous. AxoGuard® Nerve Cap is flexible and pliable to accommodate movement of the joints and surrounding soft tissues and has sufficient mechanical strength to hold appropriately sized non-absorbable suture. AxoGuard® Nerve Cap is provided sterile, for single use only, and in a variety of sizes to meet clinical needs.
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one open end, one sealed end (cap) and internal channels designed to provide protection for a peripheral nerve end or stump where repair is unattainable or not desired. The device isolates the nerve stump from the surrounding soft tissue bed by pulling the nerve into the tube and suturing the nerve within the cap. The end of the cap has a suturable tab to allow the surgeon to suture the device to surrounding tissue. AxoGuard® Nerve Cap is an extracellular matrix (ECM) and is fully remodeled during the healing process. When hydrated, AxoGuard® Nerve Cap is easy to handle, soft, pliable, nonfriable and porous. AxoGuard® Nerve Cap is flexible and pliable to accommodate movement of the joints and surrounding soft tissues and has sufficient mechanical strength to hold appropriately sized non-absorbable suture. AxoGuard® Nerve Cap is provided sterile, for single use only, and in a variety of sizes to meet clinical needs.
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one
The AxoGuard® Nerve Cap is a surgical implant that is a tubular device with one open end, one sealed end (cap) and internal channels designed to provide protection for a peripheral nerve end or stump where repair is unattainable or not desired. The device isolates the nerve stump from the surrounding soft tissue bed by pulling the nerve into the tube and suturing the nerve within the cap. The end of the cap has a suturable tab to allow the surgeon to suture the device to surrounding tissue.AxoGuard® Nerve Cap is an extracellular matrix (ECM) and is fully remodeled during the healing process. When hydrated, AxoGuard® Nerve Cap is easy to handle, soft, pliable, nonfriable and porous. AxoGuard® Nerve Cap is flexible and pliable to accommodate movement of the joints and surrounding soft tissues and has sufficient mechanical strength to hold appropriately sized non-absorbable suture. AxoGuard® Nerve Cap is provided sterile, for single use only, and in a variety of sizes to meet clinical needs.
NEUROTUBE is designed for primary or secondary peripheral nerve repair or recons
NEUROTUBE is designed for primary or secondary peripheral nerve repair or reconstruction. The NEUROTUBE device is resorbed through the process of hydrolysis.
The NEUROTUBE device Absorbable Woven Polyglycolic Acid Mesh Tube is designed fo
The NEUROTUBE device Absorbable Woven Polyglycolic Acid Mesh Tube is designed for primary or secondary peripheral nerve repair or reconstruction.
VersaWrap is an absorbable implant (device), designed to serve as an interface b
VersaWrap is an absorbable implant (device), designed to serve as an interface between target tissues and surrounding tissues to provide a non-constricting, protective encasement. VersaWrap consists of a clear Sheet and a wetting Solution. The clear Sheet is a thin membrane of crosslinked calcium alginate and glycosaminoglycan. VersaWrap Sheet is easy to handle, conformable, and is designed for placement under, around, or over injured tissues and/or surrounding tissues. VersaWrap Sheet is supplied sterile, non-pyrogenic, for single use, in double peel pouches. The VersaWrap Solution is applied to the Sheet to render the Sheet a gelatinous, tissue adherent layer (gel in situ). The aqueous citrate Solution is provided sterile, non-pyrogenic, for single use, in a dropper, packaged in a double peel pouch.