Avenue L
- Primary DI
- 03662663046534
- Brand
- Avenue L
- Company
- LDR Spine Usa, Inc.
- Model
- SI-AVEL-0089
- Catalog number
- SI-AVEL-0089
- Device description
- Angled AVENUE-L TRIAL L17 H16 0°
- Published
- 2017-03-23
- 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
Product Codes
| Code | Name |
|---|
| OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 03662663046534 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Spinal implant trial | A copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|
| Angle | 0 | degree |
| Height | 16 | Millimeter |
| Width | 17 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | Email |
|---|
| 800-699-3360 | custserv@ldrspine.com |
Regulatory Flags
- DUNS number
- 615789729
- 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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