Life Spine, Inc.
FDA 510(k) & PMA Approved Devices — 66 products
Total Devices66
Categories14
Latest FDA decision2026-07-28
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261430 | TruLift Expandable System | MAX | 2026-07-28 | View |
| 510(k) | K260571 | SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments | OLO | 2026-06-02 | View |
| 510(k) | K260837 | VersaLift Expandable System | MAX | 2026-05-12 | View |
| 510(k) | K254274 | ARx® SAI Implant System | NKB | 2026-04-16 | View |
| 510(k) | K253748 | Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System | MAX | 2026-01-23 | View |
| 510(k) | K251502 | TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System | MAX | 2025-07-07 | View |
| 510(k) | K250373 | ProLift Expandable Spacer System | MAX | 2025-04-09 | View |
| 510(k) | K243668 | ProLift Pivot Expandable Spacer System | MAX | 2025-01-23 | View |
| 510(k) | K243369 | Cervical Plating System | KWQ | 2024-12-11 | View |
| 510(k) | K242826 | ProLift Wedge Expandable Spacer System | MAX | 2024-10-08 | View |
| 510(k) | K241464 | ARx® SAI Implant System | OUR | 2024-07-29 | View |
| 510(k) | K233455 | ARx MIS Spinal Screw System | NKB | 2023-12-12 | View |
| 510(k) | K232611 | TruLift Micro Expandable Spacer System & TruLift Expandable Spacer System | MAX | 2023-11-30 | View |
| 510(k) | K231704 | Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System | OVE | 2023-10-19 | View |
| 510(k) | K223430 | ProLift Micro Expandable Spacer System | MAX | 2023-05-04 | View |
| 510(k) | K221806 | TruLift Lateral Expandable Spacer System & Lateral Plate System | MAX | 2022-12-05 | View |
| 510(k) | K222628 | Life Spine ALIF Buttress Plate System | KWQ | 2022-11-16 | View |
| 510(k) | K213417 | Ghost Spacer System | MAX | 2022-09-29 | View |
| 510(k) | K220341 | ARx Modular Spinal System | NKB | 2022-05-02 | View |
| 510(k) | K220025 | ARx® Spinal System | NKB | 2022-03-31 | View |
No matching devices.
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