AMP-LTX
- Primary DI
- 00190376601489
- Brand
- AMP-LTX
- Company
- ALPHATEC SPINE, INC.
- Model
- 622-2-101-S
- Device description
- AMP-LTX Plate, 1-Hole Left with Center Screw
- Published
- 2024-12-09
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
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 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K242147 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00190376601489 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00190376601489 | 00190376601489 | 190376601489 | 0190376601489 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal fixation plate, non-bioabsorbable | A small, implantable, non-customized sheet of solid material intended to be attached to the spine with screws for spinal immobilization; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities (e.g., during anterior/posterior cervical, anterior/posterior lumbar, thoracolumbar, and occipital fixation procedures). |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(760)431-9286 | Regulatory@alphatecspine.com |
Regulatory Flags#
- DUNS number
- 602465783
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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