AUTOVAC - AUTOGENOUS E.COLI VACCINE FOR PIGS Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

autovac - autogenous e.coli vaccine for pigs

intervet australia pty limited - autogenous e. coli vaccine for pigs - immunotherapy - pig - piglet | neonatal piglet | new born pig | sucker pig - escherichia coli scours | vaccine | equine rotavirus | white scours

Mastergraft Putty - Bone implant material, biological, animal-source Australia - English - Department of Health (Therapeutic Goods Administration)

mastergraft putty - bone implant material, biological, animal-source

medtronic australasia pty ltd - 46425 - bone matrix implant, animal-derived, bioabsorbable - mastergraft? putty is supplied as a sterile, dry, solid, construct that is hydrated for single patient use and is a mouldable form of bone void filler. mastergraft? products are biocompatible, osteoconductive, porous implants that allows for bony in growth across the graft site while resorbing at a rate consistent with bone healing. mastergraft? putty is intended to help fill voids or gaps in bone, which may be surgically created osseous defects, or osseous defects caused by traumatic injury to the bone. mastergraft? putty provides a bone void filler that is resorbed and is replaced with bone during the natural healing process. the putty when combined with either autogenous bone marrow, and/or sterile water, and/or autograft is indicated as a bone void filler for bony voids or gaps that are not intrinsic to the stability of the bony structure. additionally, mastergraft putty can be used with autograft as a bone extender. specific indications for use include oral/maxillofacial augmentation or reconstruction.

Inductos European Union - English - EMA (European Medicines Agency)

inductos

medtronic biopharma b.v. - dibotermin alfa - tibial fractures; fracture fixation, internal; spinal fusion - drugs for treatment of bone diseases - inductos is indicated for single level lumbar interbody spine fusion as a substitute for autogenous bone graft in adults with degenerative disc disease who have had at least 6 months of non operative treatment for this condition.inductos is indicated for the treatment of acute tibia fractures in adults, as an adjunct to standard care using open fracture reduction and intramedullary unreamed nail fixation.

AttraX Putty Bone Void Filler - Bone matrix implant, synthetic Australia - English - Department of Health (Therapeutic Goods Administration)

attrax putty bone void filler - bone matrix implant, synthetic

nuvasive (aust/nz) pty ltd - 17751 - bone matrix implant, synthetic - attrax putty bone void filler consists of beta tcp and hydroxyapatite in a putty form. it induces and guides the three-dimensional regeneration of bone in the defect site into which it is implanted. when placed next to viable host bone, new bone will be deposited on the surface of attrax. it then resorbs and is replaced by bone during the natural process of bone remodelling. attrax putty bone void filler is intended for use as bone void filler for voids and gaps that are not intrinsic to the stability of the bony structure. attrax is indicated for use in the treatment of surgically created osseous defects or osseous defects resulting from traumatic injury to the bone. attrax is intended to be packed into bony voids or gaps of the skeletal system (i.e., extremities, spine, and pelvis) and may be combined with autogenous bone, blood, prp, and/or bone marrow. attrax should not be used to treat large defects that in the surgeon?s opinion would fail to heal spontaneously. in load bearing situations, attrax is to b

Fixation device, internal, spine, construct Australia - English - Department of Health (Therapeutic Goods Administration)

fixation device, internal, spine, construct

globus medical australia pty ltd - 37272 - fixation device, internal, spine, construct - the revolve? stabilization system, when used as a posterior pedicle screw system, is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, pseudoarthrosis and failed previous fusion. in addition, the revolve? stabilization system is intended for treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, having implants attached to the lumbosacral spine and/or ilium with removal of the implants after attainment of a solid fusion. levels of pedicle screw fixat

Fixation device, internal, spine, construct Australia - English - Department of Health (Therapeutic Goods Administration)

fixation device, internal, spine, construct

globus medical australia pty ltd - 37272 - fixation device, internal, spine, construct - revlok? fenestrated screw system, when used as posterior pedicle screw system, is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine: degenerative disc disease (defined as discogenic back pain with degeneration of disc confirmed by history and radiographic studies), degenerative spondylolisthesis with objective evidence of neurologic impairment,fracture, dislocation, scoliosis, kyphosis, spinal tumor, pseudoarthrosis and failed previous fusion. in addition, revlok? fenestrated screw system is intended for treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, having implants attached to the lumbosacral spine and/or ilium with removal of the implants after attainment of a solid fusion. levels of pedicle screw fixation for these