ALEUTIAN® Interbody Systems
- Primary DI
- 10888857089709
- Brand
- ALEUTIAN® Interbody Systems
- Company
- K2M, INC.
- Model
- 402-90298
- Catalog number
- 402-90298
- Device description
- Horseshoe Trial, Lordotic, Size 12.5x18x13 mm
- Published
- 2016-09-16
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| MAX | Intervertebral fusion device with bone graft, lumbar |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10888857089709 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10888857089709 | 10888857089709 |
GMDN Terms
| Term | Definition |
|---|---|
| General internal orthopaedic fixation system implantation kit | A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Height | 13 | Millimeter |
| Length | 12.5 | Millimeter |
| Width | 18 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(703)777-3155 | sgilbert@k2m.com |
| +1(571)919-2000 | mark.zellers@stryker.com |
Regulatory Flags
- DUNS number
- 146060863
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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