Demineralized Bone Matrix
4D DBM Fiber
Demineralized cortical bone fibers that can be pressed into place to fill a defect. The demineralization process yields an interconnected graft matrix containing bone morphogenetic proteins and other native growth factors that support new bone growth.
Schematic representation of graft structure
Description
Demineralized cortical bone fibers, supplied loose in a range of volumes. The fibers can be pressed and packed directly into a bone void, where they interlock to form a continuous, interconnected graft matrix rather than a loose particulate fill.
Demineralization exposes bone morphogenetic proteins and other growth factors held within the cortical bone, giving the graft osteoinductive potential alongside the osteoconductive scaffold formed by the fiber network itself.
The fiber architecture rehydrates in minutes and readily takes up bone marrow aspirate, making it a practical carrier when the surgical plan calls for a composite graft.
Indications
- Craniofacial surgery
- Spinal fusion
- Hand and foot surgery
- Joint reconstruction
- Fracture repair
Benefits
- 01100% human demineralized cortical bone fiber
- 02Osteoconductive matrix
- 03Osteoinductive potential
- 04Rehydrates in minutes for ease of use
- 05Pliable and compressible handling characteristics
- 06Excellent scaffold for bone marrow aspirate
- 07Multiple graft volumes to suit a range of surgical applications
Technical Specifications
- Tissue source
- 100% human cortical bone
- Processing
- Demineralized
- Form
- Loose cortical fibers
- Volumes
- 2 cc, 5 cc, 10 cc
- Storage
- Ambient / room temperature
Ordering Information
4D DBM Fiber
| Catalog No. | Description | Size |
|---|---|---|
| 4D-F020 | DBM cortical fibers | 2 cc |
| 4D-F050 | DBM cortical fibers | 5 cc |
| 4D-F010 | DBM cortical fibers | 10 cc |
Regulatory Status
4D DBM Fiber is a human cell, tissue, or cellular and tissue-based product (HCT/P) regulated solely under Section 361 of the Public Health Service Act and 21 CFR Part 1271. It is minimally manipulated and intended for homologous use, and therefore does not require FDA pre-market approval. It has not been cleared or approved by the FDA.
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