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Orthoblast II is a powerful choice of bone grafting. It is available in both Putty and Paste form and contains demineralized bone matrix (DBM) to stimulate and regenerate new bone growth. It is a highly inductive material supplied in syringe form (smaller particulate bone granules) and in tub form (larger particulate bone granules). OrthoBlast® II combines demineralized allograft bone with cancellous bone and a reverse phase medium (RPM) to provide an osteoconductive allograft with ideal handling qualities. OrthoBlast II has enjoyed clinical success in a variety of surgical applications including periarticular defects and long-bone defects. An independent study of two DBM allografts, in cases of metaphyseal and periarticular fractures, concluded that the OrthoBlast success rate was over 30% higher than the alternative allograft product. In another independent study of the use of DBM allograft products in ankle/hindfoot fusion, 14% of patients with a glycerolbased allograft developed a nonunion, versus only 8% for the OrthoBlast patients. We offer a 24 hour delivery service for this product.
DynaGraft® II is a bone graft substitute composed of demineralized bone matrix (DBM) and a poloxamer Reverse Phase Medium (RPM) which is a biocompatible carrier. The poloxamer (RPM) turns more adhesive whilst at body temperature, providing exceptional handling and containment characteristics for surgeons. The graft is irrigation resistant, moldable, packable and can be mixed with other grafting materials. The cortical bone obtained for the demineralised bone matrix is only supplied from AATB-accredited tissue banks which is then processed into DBM in a state-of-the-art facility. As well as providing a demineralisation process, the demineralised bone matrix also undergoes Electron Beam Sterilisation which is the process of sterilising DBM and ABM under aseptic conditions.We offer a 24 hour delivery service for this product.
Accell Connexus is 2nd Generation DBM with a DBM content of close to 70%. It is sold in a syringe form and also contains the unique RPM carrier, giving it exceptional handling characteristics. Accell Connexus can be mixed with any Allograft, Autograft or a synthetic scaffold to provide the ideal recipe for fusion. Accell Technology features a patented process that produces the Accell bone matrix (ABM) which is an open-structured, dispersed form of Dynamic Bone Matrix (DBM). The ABM uses a skeletally mature sheep model with cylindrical 5mm metatarsal defect which is created in tibial diaphysis which shows results after 4 weeks. This benefits from validated osteoinductive potential, is mouldable and easy to pack into defects making it ready to use. Case studies have shown positive results when used in:
- Spine: Intertransverse process fusion
- Hand: Cystic scaphoid nonunion
- Foot & Ankle: - Tibial osteotomy - Hindfoot and ankle nonunions
Accell Connexus VarientsConnexus Putty 0.5cc - Syringe Connexus Putty 1cc – Syringe Connexus Putty 5cc – Syringe Connexus Putty 10cc – Syringe We use a guaranteed 24 hour delivery service for this product.
Allograft bone is an ideal alternative to autograft for quick, complete bone regeneration. Cancellous chips and granules form the Osteoconductive scaffold for new bone formation while maintaining the porosity essential for tissue and vascular regrowth. Cancellous Bone packs well into any size or shape defect, for maximum surgical flexibility and is available for immediate use with no refrigeration or thawing required. Potential complications of iliac crest bone harvesting, such as morbidity, limited supply, and pain, make Cancellous bone an ideal autograft substitute which has been obtained from an AATB-Accredited Tissue Bank, ensuring the highest quality bone through rigorous donor screening, testing and sterilisation. In many cases, cancellous bone is preferable to cortical bone due to its higher surface area and open porous structure that allows for easy cellular penetration and incorporation and is a perfect compliment to IsoTis’ Accell® product line, and can be used as a bone graft extender or for composite grafting. We supply Allograft Cancellous Bone in a variety of sizes which can be purchased in chip or crushed formation - please see the tab below for further information. We use a guaranteed 24 hour delivery service for this product.
The Jazz™ systems (which includes the Jazz™ Claw Connector) are temporary spinal implants specifically designed to provide a bone anchor for temporary stabilisation during the development of solid bony fusion to assist with the repair of bone fractures. The Jazz™ systems can be used for a number of spinal surgeries:
- Spinal trauma surgery
- Spinal reconstructive surgery
- Spinal degenerative surgery
Designed specifically to help the effects of Lumbar Disc Degeneration, the M6-L artificial lumbar disc is a truly innovative surgical implant which, compared to other artificial lumbar discs on the market, offers a unique design with compressive capabilities to provide a controlled range of natural motion, allowing the patient to move their back naturally. The M6-L is the world’s only artificial disc that has an incorporated artificial polycarbonate urethane nucleus and a woven polyethylene fiber annulus. Both technologies enable the M6-L to mimic the same physiologic motion characteristics of a natural disc. Spinal Kinetic have researched through extensive biomechanical testing and proven that the M6-L provides the equivalent quality of motion compared with a healthy disc. The artificial nucleus is made from a Viscoelastic polymer designed to simulate native nucleus and to provide a physiologic center of rotation. The artificial annulus is made with an Ultra High Molecular Weight Polyethylene (UHMWPE) fiber material which is designed to provide a controlled motion in all planes & axes of rotation. The M6-L is designed with two outer titanium plates featuring keels to ensure a secure anchoring of the disc into the bone. These plates are also coated with a titanium plasma spray that promotes bone growth into the metal plates to provide long-term fixation and stability of the disc in the bone.
Engineered to help the effects of Cervical Disc Degeneration, the M6 Artificial Cervical Disc provides a unique design which offers the same qualities as a natural human disc and allows for the most natural motion possible. Orthofix Announces FDA Approval of the M6-C Artificial Cervical Disc to Treat Patients with Cervical Disc Degeneration The specialist design by Spinal Kinetics means the M6 is the world’s only artificial disc with an integrated artificial polycarbonate urethane nucleus and a woven polyethylene fibre annulus. With these combined technologies, the M6 offers the most natural freedom of movement within the patient’s neck and allows for a controlled range in all 6 degrees of motion: • Vertical Translation • Lateral Translation • Anterior and Posterior Translation • Axial Rotation • Lateral Bend • Flexion Extension The artificial nucleus is made from Viscoelastic polymer which is designed to simulate the native nucleus and allow for the physiological axial compression to enable a physiological centre of rotation. The artificial annulus is made from an Ultra High Molecular Polyethylene (UHWMPE) fibre material which is designed to simulate the native annulus & its performance and provide controlled physiologic range of motion in all planes and axes. The M6 also features two outer plates made from a strong and lightweight titanium with keels to help secure the disc into the bone of the vertebral body. The plates are coated with a titanium plasma spray which helps to promote bone growth into the metal plates and offers long-term fixation and stability in the bone.
The TOPS™ System by Premia Spine is a mechanical implant device designed to offer better motion and stability for patients suffering with spinal stenosis and spondylolisthesis, offering a greater range of movement compared to Spinal Fusion technology. The unique design of the TOPS™ System allows for motion in all directions for patients including flexion, extension, lateral bending, and axial rotation. Another great feature is that the system also blocks sheer forces, which is something that can't be achieved with a typical decompression-only procedure. There are three major benefits from using the TOPS™ System as a treatment of spinal stenosis, spondylolisthesis and other facet joint diseases:
- During the procedure, the lumbar spine is stabilised and gains a controlled range of movement.
- After surgery, patients will be able to enjoy normal everyday activities by regaining the ability to bend, flex and walk.
- Once surgery is complete, patients will experience immediate and sustained pain relief according to research.
The MediExpand is a one or multi-segmental corpectomy device designed to reconstruct the cervical spine. The implant has an adjustable size increase system which can be adapted to suit the anatomical condition of the patient. Its innovative design reduces the risk of sinking adjacent vertebral bodies and secures anchoring in the adjoining endplates. Featuring an open design the mediExpand offers excellent visibility of the dura during insertion and provides direct access areas for freshening unaffected endplate areas. The large surface area is ideal for bony fusion and offers optimal space for filling up with spongiosa, whilst following the 'guide-rail' principle. The anatomical design provides the reconstruction of the lordotic profile with simple repositioning of the implant by reversing the distraction and allows for individual treatment due to the ability to choose exact height settings.
Dynamic stabilisation with the “G” Device implant for the treatment of lumbar spinal stenosis: The Device helps to support and stabilise the spine after decompression Surgery or it can be used solely as a spinal support to assist in maintaining the normal extension of the spine, thus helping to alleviate pressure on exiting nerve roots at the affected level. The advantages of the “G” Device over other similar devices is that it can be Implanted at L5/S1. It is shorter with a curved base to allow this particular level to be dealt with, and this design feature allows it to be implanted lower in the interspinous space, making it generally more stable & secure and allowing for more defined distraction. In addition, the device has clearly defined “teeth” to give it increased stability in situ.