Orthopaedics
NovioBone DBM Putty, NovioBone Foam, Cortical-Cancellous Grafts, Fascia Lata and Bone Shafts
Advanced bone matrices combine innovation with the reliability of human-derived grafts to simplify handling while promoting robust bone regeneration. Designed for complex orthopaedic procedures, these matrices provide structural integrity, enhance cellular integration, and support vascularization—critical for successful bone healing and remodeling.
Your Partner In Performance-Driven Bone Regeneration
NovioBone DBM Putty
Noviotissue introduces a next-generation solution for orthopaedic bone void filling with the NovioBone DBM Putty portfolio. Developed specifically for use in orthopaedic procedures, this portfolio offers clinicians and partners three distinct formulations, each engineered to provide excellent handling characteristics and strong regenerative potential. Manufactured in Europe and supported by proven clinical utility, NovioBone DBM Putty delivers a reliable, ready-to-use DBM solution designed to meet the demands of modern orthopaedic surgery.
Key Benefits:
- Biologically derived components
- Moldable, easy-to-handle putty consistency
- Sterile, single-use packaging
- Versatile across a wide range of orthopaedic bone regeneration procedures
4 Formulations To Fit Any Need
Not all DBM putties perform the same. NovioBone DBM Putty stands apart through formulations engineered to address the varying biological and handling demands of orthopaedic procedures. At Noviotissue, we’ve developed four distinct DBM formulations to support consistent performance across a wide range of bone regeneration scenarios.
Injectable
100% human DBM with a medium viscosity biobased carrier for smooth delivery.
Injectable +
100% human DBM with human derived carrier; a 100% human product.
Injectable Crunch
DBM with cancellous chips for added structure with a medium viscosity biobased carrier.
Paste
100% human DBM with a higher viscosity biobased carrier for better graft retention.
Local Manufacturing and Distribution
There are very few manufacturers producing DBM putty within Europe, and at NovioTissue, we see this as an opportunity to better support orthopaedic surgeons with reliable, locally produced graft solutions. By manufacturing in the EU, we bring versatile DBM formats to a growing orthopaedic market that demands consistency, availability, and performance. NovioTissue is the EU’s newest trusted source for DBM putty—made in Europe to meet the realities of modern orthopaedic surgery.
Why rely on overseas supply chains when locally produced grafts can deliver dependable availability and clinical confidence?
Every syringe of NovioBone DBM Putty is developed with orthopaedic procedures in mind:
Processed within the European Union. Manufactured under stringent quality and regulatory standards. Shorter, more reliable lead times. Trusted and transparent sourcing. Responsive support aligned with orthopaedic needs.
Regulatory Excellence and Proven Orthopaedic Performance
At NovioTissue, we’ve advanced the DBM experience for orthopaedic applications—combining refined handling, expanded formulation options, and dependable performance across a wide range of procedures. From filling contained bone voids to supporting complex reconstructions, DBM remains a cornerstone of orthopaedic bone regeneration—and now delivers greater control and consistency than ever before.
Did You Know?
DBM was originally discovered to be osteoinductive by accident in the 1960s, when researchers noticed that demineralized bone implanted into animals triggered the unexpected formation of new bone in places bone shouldn’t normally grow. That surprise finding ended up becoming one of the foundations of modern biologics.
Why does DBM continue to matter?
Because it remains a gold-standard solution in orthopaedic bone void surgery, with proven biological performance and long-standing clinical confidence.
- Osteoinductive and osteoconductive properties
- Derived from human tissue
- Backed by decades of use in orthopaedic surgical practice
Whether addressing a small defect or managing a larger bone void, NovioBone DBM Putty provides multiple formulations and volume options designed to support both routine and complex orthopaedic procedures:
- Injectable — 0.5 cc, 1.0 cc, 2.5 cc, 5.0 cc, 10 cc.
- Injectable Plus — 0.5 cc, 1.0 cc, 2.5 cc, 5.0 cc, 10 cc.
- Injectable Crunch — 0.5 cc, 1.0 cc, 2.5 cc, 5.0 cc, 10 cc.
- Paste — 0.5 cc, 1.0 cc.
Download the Product Brochure for More Information!
NovioBone DBM Putty is a 100% human-derived demineralized bone matrix engineered to support bone regeneration in orthopaedic procedures where reliability and handling are critical. Its moldable, ready-to-use consistency allows precise placement into complex or irregular bone voids, helping maintain graft position throughout the procedure. With inherent osteoconductive and osteoinductive potential, NovioBone DBM Putty provides an allograft-based scaffold that supports natural bone formation without synthetic carriers or added fillers. It is well suited for trauma, revision, and reconstructive orthopaedic applications requiring dependable defect filling and predictable healing.
NovioBone Foam
Expandable bone sponge graft designed for easy placement and secure fixation in complex orthopaedic defects and constrained anatomical spaces.
Key Benefits:
- Expandable Conformity.
- Enhanced Biological Integration.
- Efficient Handling & Time Savings.
- Structural Support in Complex Defects.
Engineered for Efficient Bone Regeneration
NovioBone Foam is specifically developed for orthopaedic use as a versatile graft solution for a wide range of bone defects. The bone sponge consists of cortico-cancellous graft particles combined with gelatine and hyaluronic acid to enhance handling and biological performance. The material can be compressed to facilitate insertion and expands upon contact with fluid, ensuring secure defect conformity and graft fixation.
This expansion increases graft porosity, enabling cell migration and vascularization, while reducing procedural steps by requiring only accurate placement. NovioBone Foam supports efficient defect filling and predictable remodeling.
Orthopaedic Applications:
Metaphyseal and epiphyseal bone defects Trauma-related bone void filling Revision and reconstructive procedures Cyst and benign lesion defect management Metaphyseal and epiphyseal bone defects Augmentation around fixation hardware
Clinical Use Cases:
Contained and non-contained bone voids Post-traumatic defect stabilization Corrective and salvage procedures Management of surgically created defects Support adjacent to plates, screws, and implants Bone void filling following implant removal
Indications For Use:
Segmental and cavitary bone defects Bone voids following fracture reduction Reconstruction and revision surgeries Defect filling after lesion removal Structural support around orthopaedic hardware Defect filling following debridement of bone tissue
Expandable graft designed for superior conformity and reliable bone regeneration.
Cortical-Cancellous Grafts
Cancellous Cubes
Engineered with both biological performance and clinical efficiency in mind, these allograft-based materials offer a natural scaffold that supports osteoconduction and osteoinduction. Their versatile handling properties make them suitable for use in trauma, spine, and reconstructive applications where traditional grafts may be difficult to place or shape. By combining strength with flexibility and biocompatibility, advanced bone matrices help surgeons achieve stable fixation and long-term graft incorporation, even in challenging anatomical sites.
Key Benefits:
- Simplified Placement.
- Secure Defect Conformity.
- Improved Biological Integration.
- Predictable Remodeling.
- Reduced Procedure Time.
Key Features:
- Compressible Sponge Format.
- Fluid-Activated Expansion.
- High-Porosity Matrix.
- Cortico-Cancellous Graft Composition.
- Ready-to-Use Design.
Clinical Applications:
- Trauma and fracture repair.
- Spinal fusion and vertebral reconstruction.
- Revision arthroplasty.
- Non-union and delayed union defects.
- Small to medium segmental defects.
Indications For Use:
- Metaphyseal and epiphyseal bone defects.
- Trauma-related bone void filling.
- Revision and reconstructive procedures.
- Defect filling following implant removal.
- Defect filling following debridement of bone tissue.
Product Handling
Cancellous Cubes can be applied directly to the defect site. Compress the cube slightly before placement; upon exposure to blood or saline, it will expand to fill the space and conform to the surrounding bone. Secure fixation is typically achieved without additional hardware.
Versatile Bone Graft for Orthopedic Reconstruction
Cancellous Cubes are designed to meet the demands of orthopedic bone repair and regeneration. Each cube acts as a dynamic bone scaffold composed of cortico-cancellous grafts integrated with gelatin and hyaluronic acid. This combination provides excellent handling, adaptability, and biological performance in both open and minimally invasive procedures.
The compressible structure allows surgeons to easily shape and position the graft into irregular bone defects. Upon contact with blood or other physiological fluids, the cubes expand—ensuring optimal defect fill, stable placement, and intimate contact with surrounding bone. The resulting increase in porosity facilitates cellular migration, angiogenesis, and new bone formation, supporting faster and more predictable healing.
Did You Know?
Cancellous cubes are so porous that they’re often compared to natural “biological sponges.” Surgeons love them because those tiny trabecular pathways act like highways for cells and blood vessels. A single cubic centimeter of cancellous bone can contain over 70 percent air space, which is one reason it integrates so well once it’s implanted.
Cancellous Granules
Noviotissue Cancellous Granules are engineered to support orthopaedic bone regeneration with a highly porous structure that mimics native cancellous bone. The interconnected trabecular architecture encourages rapid vascularization and cell migration into defect sites, facilitating osteoconduction and remodeling. These granules serve as an effective osteoconductive scaffold for filling bone voids and defects in orthopaedic procedures, supporting stable, predictable healing without the need for autograft harvest.
Key Benefits:
- Accelerated Integration.
- Osteoconductive Scaffold.
- Versatile Application.
- Predictable Remodeling.
- Ready‑to‑Use Handling.
Highly porous and easy to handle, Cancellous Granules provide clinicians with a reliable, ready-to-use scaffold for consistent, effective bone regeneration in orthopaedic procedures.
Seamless Scaffold for Biological Ingrowth
Cancellous Granules deliver a biologically active scaffold that supports rapid vascularization and cellular infiltration, enabling the host bone to regenerate efficiently. The trabecular‑like porous structure provides an osteoconductive environment, promoting bone deposition while allowing remodeling over time. Ready to use and simple to place, these granules help clinicians address a wide variety of orthopaedic bone voids without the morbidity associated with autograft harvest.
Key Features:
- Highly Porous Architecture.
- Osteoconductive Material.
- Consistent Granule Size.
- Biocompatible Allograft Matrix.
- Ready‑to‑Use Format.
Clinical Applications:
- Long bone trauma reconstruction.
- Pelvic and acetabular defect filling.
- Proximal humerus and tibial plateau defects.
- Non‑union and delayed union support.
- Adjunct in bone grafting with internal fixation.
Indications For Use:
- Traumatic bone void filling.
- Metaphyseal defect management.
- Bone grafting in non‑union sites.
- Defect filling after tumor or cyst excision.
- Supporting bone healing in fracture repair.
Cortical Cancellous Blend (50/50)
Noviotissue Cortical‑Cancellous Blend (50/50) is formulated to provide a balanced osteoconductive scaffold for orthopaedic bone regeneration. By combining the relative structural support of cortical bone with the porosity of cancellous bone, this blended graft offers space maintenance and faster biological integration. The result is a versatile material suitable for a broad range of orthopaedic defects where both mechanical stability and biological performance are important for healing and remodeling.
Key Benefits:
- Balanced Structural Support.
- Facilitated Biological Integration.
- Osteoconductive.
- Predictable Healing.
- Streamlined Handling.
Balanced support and accelerated biological regeneration in a ready‑to‑use bone graft for orthopaedic reconstruction.
Enhanced Scaffold for Strength and Healing
Noviotissue Cortical‑Cancellous Blend (50/50) delivers a unified graft matrix that balances structural maintenance with biologic responsiveness. The cortical portion helps support defect geometry and early stability, while the cancellous component’s porosity encourages revascularization and cell migration. This tailored balance enables clinicians to address a wide array of orthopaedic bone voids with a single, ready‑to‑use graft designed for efficient placement and predictable integration.
Key Features:
- 50/50 Cortical‑Cancellous Mix.
- Interconnected Porosity.
- Osteoconductive Matrix.
- Consistent Particle Size.
- Ready-to-Use Format.
Clinical Applications:
- Fracture non‑union and delayed union therapy.
- Pelvic and acetabular defect reconstruction.
- Tibial and femoral plateau defect management.
- Bone loss following hardware removal or revision.
- Adjunct to internal fixation in complex trauma.
Indications For Use:
- Bone void filling in long bone defects.
- Support in metaphyseal and epiphyseal defects.
- Grafting adjacent to hardware in fracture repair.
- Defect filling following cyst or tumor excision.
- Supplemental grafting in reconstructive procedures.
Fascia Lata
Discover how advanced biologic materials can enhance orthopedic outcomes. This section provides the insights you need to make confident clinical decisions, highlighting the science behind materials that support reliable bone and tissue healing. Compare autologous and allograft sources to understand how each contributes to musculoskeletal repair, and explore the differences between decellularization and sterilization techniques that ensure safety while preserving the regenerative potential of fascia lata and other grafts from NovioTissue.
Balanced support and accelerated biological regeneration in a ready‑to‑use bone graft for orthopaedic reconstruction.
Natural Integration
Using biologic materials like fascia lata has been shown to enhance graft integration with host musculoskeletal tissue, supporting more predictable orthopedic healing.
Minimal Inflammation
These materials help reduce postoperative inflammatory responses, promoting a smoother recovery after implantation.
Material Options
Orthopedic grafts are available in two main types: Autograft (patient-derived) and Allograft (donor-derived, including products from NovioTissue).
Autologous vs. Allograft Tissues
Autografts
Allografts
Pros:
- Risk of rejection is minimal.
- Easy acceptance of the graft at the host site.
Cons:
- Donor-site morbidity.
- Post-operative pain of several months.
- Cosmetic concerns regarding scar formation.
- More complex anesthesia and surgery time.
Pros:
- Risk of rejection is minimal compared to synthetic material.
- No donor-site morbidity.
- No discomfort associated with harvesting the autograft.
- Less surgery time, no double surgeries.
Cons:
- Processing and sterilization conditions to reduce risk of rejection.
- Mechanical properties are slightly lower.
Comparison of Allograft Materials
Dermal
Fascia Lata
Pros:
- Dense collagen fibers provide acceptable tensile strength and mechanical properties.
- Good initial flexibility.
Cons:
- High collagen density makes them nearly non-porous, which can limit host cell integration.
- Tissue union may be suboptimal.
- Mechanical properties tend to decrease over time, reducing long-term structural support.
Pros:
- More porous than dermal tissue, promoting superior tissue integration and union.
- Demonstrates high and consistent tensile strength for orthopedic applications.
- Maintains long-term mechanical stability, supporting reliable musculoskeletal repair.
Cons:
- Less flexible than dermal allografts, though strength and integration advantages often outweigh this.
- Higher cost compared to other allograft options.
Why Does Fascia Lata Tissue Outperform Dermal Tissue?
- Biomechanical Advantages:
Fascia lata is a collagen-rich, strap-like tissue engineered to resist tensile loads in musculoskeletal applications. Unlike dermal tissue, it does not rely heavily on elastin networks for strength. Even after processing, fascia lata maintains its mechanical integrity, providing long-term durability under repeated orthopedic stresses such as tendon repair, ligament reconstruction, and load-bearing joint support. - Dermis Limitations:
Dermal tissue contains both collagen and elastic fibers; however, elastin deteriorates with age—fibers fragment, shorten, and fibroblasts produce less tropoelastin. Tissue banks often source dermis from older donors, meaning grafts arrive with pre-degraded elastin. Processing methods—such as solvent dehydration, detergents, and gamma irradiation—further compromise collagen ultrastructure and elasticity. Clinically, dermal grafts can provide reinforcement or coverage, but under constant orthopedic loads they may stretch, lose tension, and compromise structural support over time. - Clinical Evidence:
In orthopedic procedures, fascia lata allografts demonstrate consistent long-term mechanical performance, excellent tissue integration, and reliable outcomes in tendon and ligament reconstructions. Dermal grafts, while safe and biologically compatible, show reduced mechanical resilience under chronic load, potentially leading to elongation or diminished support in high-stress applications. - Processing Matters:
Maintaining the structural and functional integrity of fascia lata through careful processing ensures that orthopedic surgeons can rely on predictable graft performance, long-term strength, and durable musculoskeletal repair.
Decellularization and Sterilization Technique
Fascia Lata from NovioTissue is a lyophilized sheet processed under stringent quality and aseptic control standards. This ensures minimal or no residual debris, effectively removing organic material (lipids, blood) and inactivating any microorganisms, making it safe and reliable for orthopedic applications.
✅ Fascia Lata
- Longer shelf life for the graft.
- Enhanced cell adhesion, promoting superior tissue integration once implanted.
- Preservation of tissue tensile strength, as scCO₂ processing does not alter the tissue structure.
Step 1: Decellularization
Step 2: Sterilization
Step 3: Outcome
Thorough dehydration extends graft shelf life and prepares the tissue for optimal use.
scCO₂ decellularization and sterilization remove donor DNA without altering fiber surfaces or tissue structure, ensuring predictable mechanical performance in orthopedic repairs.
❌ Other Allografts
- Cell adhesion may be compromised due to fiber erosion, resulting in suboptimal tissue integration.
- Reduced tensile strength from fiber breakage and unnatural collagen crosslinking.
Step 1: Decellularization
Step 2: Sterilization
Step 3: Outcome
Limited dehydration using solvents, which can impact long-term graft stability.
Gamma irradiation significantly alters tissue structure, potentially reducing mechanical performance and long-term durability in orthopedic applications.
Supercritical CO₂ vs. Gamma-Irradiation
Supercritical CO₂ (scCO₂) is an advanced sterilization method that provides a gentle yet effective approach for orthopedic tissue processing. While gamma irradiation can degrade the mechanical properties of grafts, scCO₂ sterilizes tissue without significantly affecting its structural integrity. Comparative studies show that scCO₂-treated allografts maintain both safety and long-term performance, making them ideal for musculoskeletal applications.
Benefits of scCO₂ in Allograft’s Clinical Performance
Sterilizing allograft tissue with scCO₂ offers several advantages over conventional methods such as gamma irradiation, steam sterilization, or ethylene oxide (EtO):
- Achieves effective sterilization with a Sterility Assurance Level (SAL) of 10⁻⁶.
- Preserves the tensile strength of the graft.
- Does not chemically react with the tissue, avoiding unwanted collagen crosslinking or increased stiffness.
scCO₂
- Excellent penetration throughout orthopedic graft tissue.
- Maintains tensile strength and mechanical integrity after sterilization.
Gamma Irradiation:
- Alters graft structure, compromising performance in orthopedic repairs.
- Significantly reduces tensile strength under musculoskeletal loads.
- Generates free radicals, potentially affecting patient safety.
CaseStudies
Processing Differences (scCO₂ vs Gamma)
- Schmid R, et al. Supercritical CO₂ sterilization preserves biomechanical properties of tendon allografts compared with gamma irradiation. J Orthop Res. 2017.
- Oberringer M, et al. Supercritical carbon dioxide–based decellularization and sterilization of dense connective tissues. Biomed Mater. 2018.
Resources
Browse this abstract for a quick insight into the ideas, research, and innovations shaping the field. Each summary highlights the essentials, making it easy to discover what matters most before diving deeper.
Effects of Supercritical Fluid CO₂ and 25 kGy Gamma Irradiation on the Initial Mechanical Properties and Histological Appearance of Tendon Allograft.
This study compares two sterilization methods—supercritical CO₂ and gamma irradiation—on tendon allografts. Findings show that gamma irradiation weakens tendon structure and mechanical strength, while supercritical CO₂ preserves biomechanical properties and tissue integrity, suggesting it as a safer alternative for graft preparation.
Bone Shafts
Bone shafts are structural allograft implants designed to restore segmental bone loss and provide immediate mechanical stability in complex orthopaedic reconstructions. Comprised of dense cortical and cancellous human bone, these grafts function as load-bearing scaffolds while supporting biological integration and remodeling as healing progresses. Bone shafts are available across multiple long-bone anatomies to accommodate a variety of surgical needs, including:
- Femoral shafts
- Tibial shafts
- Fibular shafts
- Humeral shafts
Key Benefits:
- Restores load-bearing stability in large segmental defects.
- Eliminates donor-site morbidity associated with autograft harvest.
- Supports predictable integration and long-term remodeling.
- Reduces intraoperative preparation time.
- Adaptable across a wide range of orthopaedic reconstructions.
Processing and Sterilization
Bone shafts are processed using validated cleaning and sterilization methods designed to reduce bioburden while preserving the graft’s structural and biological properties. Sterility assurance levels (SAL) of up to 10⁻⁶ are achieved without compromising osteoconductive performance
Key Features:
- Structural cortical bone composition.
- Osteoconductive natural matrix.
- 100% human allograft.
- Multiple anatomical configurations.
- Sterile, clinically validated processing
Clinical Applications:
- Segmental bone defect reconstruction.
- Orthopaedic oncology reconstruction.
- Complex trauma repair.
- Revision and salvage procedures.
- Deformity correction support
Indications For Use:
- Restoration of long-bone continuity.
- Structural support following bone loss.
- Reinforcement in nonunion repair.
- Reconstruction after tumor resection.
- Load-bearing grafting applications.
Order Information
Use the following information when filling out your purchase order. To obtain individual/box-quantity pricing, or to submit a purchase order, contact your local distributor. To find a local distributor, submit a contact form on our contact us page.
Code | Description | Diameter / Dimensions / Volume | Thickness |
NT1005FD | NovioBone DBM Putty Injectable; 100% DBM with Biobased Carrier | 0.5 CC | Medium Viscosity |
NT1020FD | NovioBone DBM Putty Injectable; 100% DBM with Biobased Carrier | 1.0 CC | Medium Viscosity |
NT1025FD | NovioBone DBM Putty Injectable; 100% DBM with Biobased Carrier | 2.5 CC | Medium Viscosity |
NT1050FD | NovioBone DBM Putty Injectable; 100% DBM with Biobased Carrier | 5.0 CC | Medium Viscosity |
NT1060FD | NovioBone DBM Putty Injectable; 100% DBM with Biobased Carrier | 10.0 CC | Medium Viscosity |
NT1505FD | NovioBone DBM Putty Injectable Plus; 100% DBM with Human Carrier | 0.5 CC | Medium Viscosity |
NT1510FD | NovioBone DBM Putty Injectable Plus; 100% DBM with Human Carrier | 1.0 CC | Medium Viscosity |
NT1525FD | NovioBone DBM Putty Injectable Plus; 100% DBM with Human Carrier | 2.5 CC | Medium Viscosity |
NT1550FD | NovioBone DBM Putty Injectable Plus; 100% DBM with Human Carrier | 5.0 CC | Medium Viscosity |
NT1560FD | Injectable Plus; 100% DBM with Human Carrier | 10.0 CC | Medium Viscosity |
NT1105FD | NovioBone DBM Putty Injectable Crunch; 100% DBM and Cancellous with Biobased Carrier | 0.5 CC | Medium Viscosity |
NT1110FD | NovioBone DBM Putty Injectable Crunch; 100% DBM and Cancellous with Biobased Carrier | 1.0 CC | Medium Viscosity |
NT1125FD | NovioBone DBM Putty Injectable Crunch; 100% DBM and Cancellous with Biobased Carrier | 2,5 CC | Medium Viscosity |
NT1150FD | NovioBone DBM Putty Injectable Crunch;100% DBM and Cancellous with Biobased Carrier | 5.0 CC | Medium Viscosity |
NT1160FD | NovioBone DBM Putty Injectable Crunch;100% DBM and Cancellous with Biobased Carrier | 10.0 CC | Medium Viscosity |
NT1205FD | NovioBone DBM Putty Paste; 100% DBM with Biobased Carrier | 0.5 CC | High Viscosity |
NT1210FD | NovioBone DBM Putty Paste; 100% DBM with Biobased Carrier | 1.0 CC | High Viscosity |
NT1220FD | NovioBone DBM Putty Paste; 100% DBM with Biobased Carrier | 2.0 CC | High Viscosity |
NT1225FD | NovioBone DBM Putty Paste; 100% DBM with Biobased Carrier | 2.5 CC | High Viscosity |
NT1250FD | NovioBone DBM Putty Paste; 100% DBM with Biobased Carrier | 5.0 CC | High Viscosity |
NT1260FD | NovioBone DBM Putty Paste; 100% DBM with Biobased Carrier | 10.0 CC | High Viscosity |
NT2001FD | NovioBone Foam D, Freeze Dried | 12 MM | 9 MM |
NT2002FD | NovioBone Foam K1, Freeze Dried | 25 MM | 9 MM |
NT2003FD | NovioBone Foam K2, Freeze Dried | 30 MM | 10 MM |
NT2004FD | NovioBone Foam S1, Freeze Dried | 15 x 3.5 MM | 10 MM |
NT2005FD | NovioBone Foam S2, Freeze Dried | 6 x 3 MM | 10 MM |
NT0040FD | NovioBone Cancellous Cubes | 10 x 10 MM | 10 MM |
NT0041FD | NovioBone Cancellous Cubes | 10 x 10 MM | 20 MM |
NT0042FD | NovioBone Cancellous Cubes | 10 x 20 MM | 20 MM |
NT0043FD | NovioBone Cancellous Cubes | 20 x 20 MM | 30 MM |
NT0011FD | NovioBone Cancellous Granules | 0.5 CC | 1.0 – 4.0 MM |
NT0012FD | NovioBone Cancellous Granules | 1.0 CC | 1.0 – 4.0 MM |
NT0013FD | NovioBone Cancellous Granules | 2.0 CC | 1.0 – 4.0 MM |
NT0014FD | NovioBone Cancellous Granules | 5.0 CC | 1.0 – 4.0 MM |
NT0015FD | NovioBone Cancellous Granules | 10.0 CC | 1.0 – 4.0 MM |
NT0021FD | NovioBone Cancellous Granules | 0.5 CC | 4.0 – 10.0 MM |
NT0022FD | NovioBone Cancellous Granules | 1.0 CC | 4.0 – 10.0 MM |
NT0023FD | NovioBone Cancellous Granules | 2.0 CC | 4.0 – 10.0 MM |
NT0024FD | NovioBone Cancellous Granules | 5.0 CC | 4.0 – 10.0 MM |
NT0025FD | NovioBone Cancellous Granules | 10.0 CC | 4.0 – 10.0 MM |
NT0026FD | NovioBone Cancellous Granules | 15.0 CC | 4.0 – 10.0 MM |
NT0030FD | NovioBone Cortico-Cancellous Blend (50/50) | 5.0 CC | 1.0 – 4.0 MM |
NT0031FD | NovioBone Cortico-Cancellous Blend (50/50) | 10.0 CC | 1.0 – 4.0 MM |
NT0032FD | NovioBone Cortico-Cancellous Blend (50/50) | 15.0 CC | 1.0 – 4.0 MM |
NT0035FD | NovioBone Cortico-Cancellous Blend (50/50) | 5.0 CC | 4.0 – 10.0 MM |
NT0036FD | NovioBone Cortico-Cancellous Blend (50/50) | 10.0 CC | 4.0 – 10.0 MM |
NT0037FD | NovioBone Cortico-Cancellous Blend (50/50) | 15.0 CC | 4.0 – 10.0 MM |
NT2108FD | Amnion* Disc – S, Freeze Dried | 8 MM | 0.1 MM |
NT2110FD | Amnion* – M, Freeze Dried | 10 x 10 MM | 0.1 MM |
NT2010FD | Amnion* Disc – M, Freeze Dried | 10 MM | 0.1 MM |
NT2012FD | Amnion* Disc – L, Freeze Dried | 12 MM | 0.1 MM |
NT2120FD | Amnion* – L, Freeze Dried | 20 x 20 MM | 0.1 MM |
NT2016FD | Amnion* Disc – XL Freeze Dried | 16 MM | 0.1 MM |
NT2060FD | Amnion* – XL, Freeze Dried | 20 x 30 MM | 0.1 MM |
NT1010FD | Dermis – M, Freeze Dried | 10 MM | 0.2 MM |
NT1016FD | Dermis – L, Freeze Dried | 16 MM | 0.2 MM |
NT1030FD | Dermis – XL, Freeze Dried | 25 x 30 MM | 0.2 MM |
BE####0FD | Femur Shaft | 10 – 15 MM | – |
NT####0FD | Femur Shaft | 16 – 30 MM | – |
NT####0FD | Femur Shaft | 31 – 50 MM | – |
NT####0FD | Fibula Shaft | 5 – 10 MM | – |
NT####0FD | Fibula Shaft | 11 – 20 MM | – |
NT####0FD | Fibula Shaft | 21 – 30 MM | – |
NT####0FD | Humeral Shaft | 15 – 30 MM | – |
NT####0FD | Humeral Shaft | 31 – 50 MM | – |
NT####0FD | TibialShaft | 20 – 40 MM | – |
NT####0FD | Cortical Strut Single | 50 – 100 MM | – |
NT####0FD | Cortical Strut Double | 50 – 100 MM | – |
NT####0FD | Cortical Shaft Hemi Femoral | 30 – 50 MM | – |
NT####0FD | Cortical Shaft Hemi Tibial | 30 – 50 MM | – |
* Medtronic EpiDisc and EpiFilm Replacement | |||