AlphaGRAFT
- Primary DI
- 00844856026728
- Brand
- AlphaGRAFT
- Company
- ALPHATEC SPINE, INC.
- Model
- 1002-025
- Device description
- AlphaGRAFT, Bone Matrix Putty, Demineralized, 2.5cc
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| MBP | Filler, bone void, osteoinduction (w/o human growth factor) |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| MBP | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00844856026728 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00844856026728 | 00844856026728 | 844856026728 | 0844856026728 |
GMDN Terms
| Term | Definition |
|---|---|
| Bone matrix implant, human-derived | An sterile implantable device made primarily of human demineralized bone matrix (DBM) (acid extraction of allogeneic bone resulting in loss of most of the mineralized component but retention of proteins) intended to fill bony voids or gaps caused by trauma or surgery, including use in the maxillofacial and/or mandibular bone. The device is bioabsorbable, osteoconductive, and has demonstrated at least potential osteoinductivity for the stimulation of new bone growth. The DBM may be combined with various carrier compounds (e.g., gelatin, hydrogel, starch) or other materials. It is available in the form of powder, crushed granules, putty, chips, or a gel that can be injected through a syringe. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Total Volume | 2.5 | Milliliter |
Sterilization Methods
| Method |
|---|
| Radiation Sterilization |
Regulatory Flags
- DUNS number
- 602465783
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- false
- HCT/P
- true
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- true
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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