GoPLF! Posterior Lateral Fusion Device
- Primary DI
- 07640387660652
- Brand
- GoPLF! Posterior Lateral Fusion Device
- Company
- GetSet Surgical SA
- Model
- 3201100
- Device description
- GoPLF! Posterior Lateral Fusion Device, 5.5mm x 100mm Straight Ti rods-2 per pack
- Published
- 2023-12-12
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| NKB | Thoracolumbosacral Pedicle Screw System |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| NKB | Thoracolumbosacral Pedicle Screw System | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 07640387660249 | Primary | GS1 | 0 | |
| 07640387660652 | Unit of Use | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 07640387660249 | 07640387660249 | 7640387660249 |
| 07640387660652 | 07640387660652 | 7640387660652 |
GMDN Terms
| Term | Definition |
|---|
| Bone-screw internal spinal fixation system, sterile | An assembly of sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Sterile disposable devices associated with implantation may be included. |
Regulatory Flags
- DUNS number
- 480143831
- Device count
- 2
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|
| 07640387660270 | GoLIF! Lumbar Interbody Fusion System | 3102208 | | 2025-04-01 |
| 07640387660287 | GoLIF! Lumbar Interbody Fusion System | 3102209 | | 2025-04-01 |
| 07640387660294 | GoLIF! Lumbar Interbody Fusion System | 3102210 | | 2025-04-01 |
| 07640387660300 | GoLIF! Lumbar Interbody Fusion System | 3102211 | | 2025-04-01 |
| 07640387660317 | GoLIF! Lumbar Interbody Fusion System | 3102212 | | 2025-04-01 |
| 07640387660324 | GoLIF! Lumbar Interbody Fusion System | 3102213 | | 2025-04-01 |
| 07640387660331 | GoLIF! Lumbar Interbody Fusion System | 3102214 | | 2025-04-01 |
| 07640387660348 | GoLIF! Lumbar Interbody Fusion System | 3102608 | | 2025-04-01 |
| 07640387660355 | GoLIF! Lumbar Interbody Fusion System | 3102609 | | 2025-04-01 |
| 07640387660362 | GoLIF! Lumbar Interbody Fusion System | 3102610 | | 2025-04-01 |
| 07640387660379 | GoLIF! Lumbar Interbody Fusion System | 3102611 | | 2025-04-01 |
| 07640387660386 | GoLIF! Lumbar Interbody Fusion System | 3102612 | | 2025-04-01 |
| 07640387660393 | GoLIF! Lumbar Interbody Fusion System | 3102613 | | 2025-04-01 |
| 07640387660409 | GoLIF! Lumbar Interbody Fusion System | 3102614 | | 2025-04-01 |
| 07640387660843 | GoLIF! Lumbar Interbody Fusion System | 4020001 | | 2025-04-01 |
| 07640387660850 | GoLIF! Lumbar Interbody Fusion System | 4020002 | | 2025-04-01 |
| 07640387660478 | GoPLF! Posterior Lateral Fusion Device | 3206545 | | 2023-12-12 |
| 07640387660485 | GoPLF! Posterior Lateral Fusion Device | 3206550 | | 2023-12-12 |
| 07640387660492 | GoPLF! Posterior Lateral Fusion Device | 3206555 | | 2023-12-12 |
| 07640387660508 | GoPLF! Posterior Lateral Fusion Device | 3207535 | | 2023-12-12 |
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