Ldr Spine USA, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2017-05-16
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K162133 | VerteFIT Corpectomy Cage System | MQP | 2017-05-16 | View |
| 510(k) | K161173 | Avenue® T TLIF Cage | OVD | 2016-09-28 | View |
| 510(k) | K161798 | FacetBRIDGE® System | MRW | 2016-08-04 | View |
No matching devices.