OsteoFlo HydroFiber - 6cc Labeled
- Primary DI
- 00810131881443
- Brand
- OsteoFlo HydroFiber - 6cc Labeled
- Company
- Surgentec, LLC
- Model
- HF-OSF-06
- Published
- 2026-03-09
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Rx
- true
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| MQV | Filler, Bone Void, Calcium Compound |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MQV | Filler, Bone Void, Calcium Compound | Orthopedic | 2 |
Premarket Submissions#
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00810131881443 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00810131881443 | 00810131881443 | 810131881443 | 0810131881443 |
GMDN Terms#
| Term | Definition |
|---|---|
| Vertebral bone filler, bioabsorbable | A sterile substance intended to be used to replace cortical/cancellous bone in a vertebral body to stabilize vertebral compression fractures (VCFs) caused by cancer, osteoporosis, or trauma. The device is typically a sterile powder made of a calcium compound (e.g., calcium phosphate, calcium carbonate, hydroxyapatite), that is mixed with its sterile diluent prior to implantation, and designed to be implanted during a balloon kyphoplasty or vertebroplasty procedure. This device does not contain an antibiotic agent. After application, this device cannot be reused. |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 004095409
- Device count
- 1
- Lot or batch
- true
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00810131882433 | ION-C Navigation Locator | SR12-2512 | 2026-07-06 | |
| 00810131882440 | Ion Navigation Drill Bit - 5.0mm | SR12-6510 | 2026-07-06 | |
| 00810131882457 | Ion Navigation Drill Bit - 5.5mm | SR12-6511 | 2026-07-06 | |
| 00810131882464 | Ion Navigation Drill Bit - 4.5mm | SR12-6509 | 2026-07-06 | |
| 00810131882532 | TiLink-L Navigation Drill Bit - 8mm | SR21-6305 | 2026-07-06 | |
| 00810131882556 | TiLink-L Navigation Drill Guide | SR21-6301 | 2026-07-06 | |
| 00810131882563 | TiLink-L Navigation Inserter Hexalobe Driver | SR21-6304 | 2026-07-06 | |
| 00810131882617 | TiLink-L Navigation Impact Cap | SR21-6303 | 2026-07-06 | |
| 00810131882761 | Facet Sterile Implant - 55 | FI-S-55 | 2026-07-06 | |
| 00810131882808 | Facet Sterile Instrument Kit - Cervical | FIC-1000 | 2026-07-06 | |
| 00810131883270 | ION-C Navigation Drill Guide - Adjustable | SR12-2700 | 2026-07-06 | |
| 00810131883669 | Ion Navigation Inserter AO | SR12-6501 | 2026-07-06 | |
| 00810131884772 | ION-C Final Kit | TI-C-1000 | 2026-07-06 | |
| 00810131884871 | ION-C Navigation Reusable Tray | SR25-7005 | 2026-07-06 | |
| 00810131884895 | ION-C Reusable | SR25-1000 | 2026-07-06 | |
| 00810131884970 | ION-C Navigation Reusable Tray Assembly | SR25-1002 | 2026-07-06 | |
| 00810131881061 | BMAC Bevel Needle | SR07-1500 | AAN-11-BMACS | 2025-01-03 |
| 00810131880941 | BMAN Solid Diamond Needle | SR07-1100 | AAN-09-BMANS | 2024-12-31 |
| 00810131880958 | BMAN Solid Diamond Needle Kit | SR07-1101 | AAN-09-BMAN | 2024-12-31 |
| 00810131880965 | BMAN Solid Diamond Needle - Two Pack | SR07-1102 | AAN-09-2BMANS | 2024-12-31 |
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|---|---|---|---|---|
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| 00816125027132 | VitaFuse™ Bioactive Glass Graft | BERKELEY ADVANCED BIOMATERIALS, LLC | MQV | 2026-07-06 |
| 00816125027149 | VitaFuse™ Bioactive Glass Graft | BERKELEY ADVANCED BIOMATERIALS, LLC | MQV | 2026-07-06 |
| W4184058150T0474 | DBX® | Musculoskeletal Transplant Foundation, Inc. | MQV | 2026-06-05 |
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| 03760191134850 | AktiBone Granules | NORAKER | MQV | 2026-05-27 |
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