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) | K191005 | ProLift® Expandable System | MAX | 2019-06-13 | View |
| 510(k) | K183430 | Modular Spinal Fixation System | NKB | 2019-03-13 | View |
| 510(k) | K181625 | Life Spine Resolute™ Threaded Cage System | MAX | 2018-12-11 | View |
| 510(k) | K181717 | Life Spine Laminoplasty System | NQW | 2018-10-12 | View |
| 510(k) | K180215 | DYNA-LINK ELITE Stand-Alone Anterior Lumbar System | OVD | 2018-09-13 | View |
| 510(k) | K173883 | External Fixation System | KTT | 2018-09-07 | View |
| 510(k) | K180166 | Life Spine Lumbar Fixation System (SENTRY) | KWQ | 2018-06-22 | View |
| 510(k) | K180749 | Life Spine SIMPACT Sacroiliac Joint Fixation System | OUR | 2018-06-15 | View |
| 510(k) | K180642 | Pro-Link® Ti Stand-Alone Cervical Spacer System | OVE | 2018-05-10 | View |
| 510(k) | K172105 | The Plateau-LO Spacer System | MAX | 2018-02-02 | View |
| 510(k) | K173047 | The Solstice OCT System | NKG | 2018-02-01 | View |
| 510(k) | K172973 | Life Spine Foot and Ankle Plating System | HRS | 2017-12-21 | View |
| 510(k) | K173182 | ProLift® Expandable System | MAX | 2017-12-20 | View |
| 510(k) | K173286 | Cannulated Screw Internal Fixation System | HWC | 2017-12-14 | View |
| 510(k) | K172131 | 2 Hole Lateral Plating System | KWQ | 2017-08-28 | View |
| 510(k) | K170919 | The TiBow Expandable Spacer System | MAX | 2017-08-03 | View |
| 510(k) | K171448 | Hammertoe Correction System | HWC | 2017-07-07 | View |
| 510(k) | K162685 | 2-Piece Hammertoe Correction System | HWC | 2017-06-09 | View |
| 510(k) | K170804 | The Solstice OCT System | NKG | 2017-05-18 | View |
| 510(k) | K162266 | The Cranial Fusion System | NKG | 2017-05-01 | View |
No matching devices.
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