ALTA STAND-ALONE INTERBODY FUSION SYSTEM
- Primary DI
- 00888480556015
- Brand
- ALTA STAND-ALONE INTERBODY FUSION SYSTEM
- Company
- BIOMET SPINE LLC
- Model
- 8417-0012
- Catalog number
- 8417-0012
- Published
- 2015-10-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| OVE | Intervertebral fusion device with integrated fixation, cervical |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888480556015 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888480556015 | 00888480556015 | 888480556015 | 0888480556015 |
GMDN Terms#
| Term | Definition |
|---|---|
| Polymeric spinal interbody fusion cage | A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)447-3625 | USBROCustomerService@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 018577570
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00880304860544 | Vitality®+ Osteotomy | 732M2129 | 732M2129 | 2018-06-05 |
| 00880304860551 | Vitality®+ Osteotomy | 732M2221 | 732M2221 | 2018-06-05 |
| 00880304860568 | Vitality®+ Osteotomy | 732M2224 | 732M2224 | 2018-06-05 |
| 00880304860575 | Vitality®+ Osteotomy | 732M2226 | 732M2226 | 2018-06-05 |
| 00880304860582 | Vitality®+ Osteotomy | 732M2229 | 732M2229 | 2018-06-05 |
| 00888480489450 | LINEUM OCT SPINE SYSTEM | 14-525013 | 14-525013 | 2020-10-15 |
| 00888480511564 | LINEUM OCT SPINE SYSTEM | 14-525054 | 14-525054 | 2020-07-07 |
| 00888480207542 | POLARIS 5.5 SPINAL SYSTEM | 2000-2325 | 2000-2325 | 2015-10-24 |
| 00880304964143 | Polaris™ 6.35 Spinal System | 14-513730R | 14-513730R | 2020-11-10 |
| 00880304964433 | Polaris™ 6.35 Spinal System | 14-513555R | 14-513555R | 2020-11-10 |
| 03662663058155 | Spine System | 14-500771 | 14-500771 | 2021-12-17 |
| 03662663058162 | Spine System | 14-500772 | 14-500772 | 2021-12-17 |
| 03662663058179 | Spine System | 14-500773 | 14-500773 | 2021-12-17 |
| 03662663058186 | Spine System | 14-500774 | 14-500774 | 2021-12-17 |
| 03662663058193 | Spine System | 14-500775 | 14-500775 | 2021-12-17 |
| 03662663058209 | Spine System | 14-500776 | 14-500776 | 2021-12-17 |
| 03662663058216 | Spine System | 14-500777 | 14-500777 | 2021-12-17 |
| 03662663058223 | Spine System | 14-500778 | 14-500778 | 2021-12-17 |
| 03662663058230 | Spine System | 14-500779 | 14-500779 | 2021-12-17 |
| 03662663058247 | Spine System | 14-500780 | 14-500780 | 2021-12-17 |
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