Demineralized Bone Matrix
4D DBM Putty
A malleable demineralized bone matrix putty formulated to resist irrigation. Supplied in volumes covering procedures from foot and ankle through trauma, extremities, knee, hip, craniomaxillofacial and spine.
Schematic representation of graft structure
Description
A cohesive, mouldable demineralized bone matrix putty that can be shaped by hand and pressed into irregular defects without preparation or mixing.
The putty is formulated to resist irrigation, which keeps the graft in position through lavage and closure rather than migrating out of the site.
Available volumes are intended to cover a broad procedural range, including foot and ankle, trauma and extremities, knee, hip, craniomaxillofacial and spine. Demineralized bone matrix may be used to supplement autologous cancellous or corticocancellous graft material.
Indications
- Craniofacial surgery
- Spinal fusion
- Hand and foot surgery
- Joint reconstruction
- Fracture repair
Benefits
- 01Easy to use
- 02Open and go — no preparation required
- 03Malleable and shapeable by hand
- 04Resists irrigation and stays in place
- 05Osteoconductive and osteoinductive potential
Technical Specifications
- Form
- Malleable putty
- Handling
- Resists irrigation
- Volumes
- 1 cc, 2.5 cc, 5 cc, 10 cc
- Preparation
- None — open and go
- Storage
- Ambient / room temperature
Ordering Information
4D DBM Putty
| Catalog No. | Description | Size |
|---|---|---|
| 4D-HG-01P | DBM putty | 1 cc |
| 4D-HG-02P | DBM putty | 2.5 cc |
| 4D-HG-05P | DBM putty | 5 cc |
| 4D-HG-10P | DBM putty | 10 cc |
Regulatory Status
4D DBM Putty 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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