Ldr Spine USA, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 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 |
| 510(k) | K123134 | EASYSPINE SYSTEM | NKB | 2013-02-01 | View |
| 510(k) | K121103 | LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S | NKB | 2012-08-24 | View |
| 510(k) | K113285 | LDR SPINE USA AVENUE L INTERBODY FUSION | OVD | 2012-07-26 | View |
| 510(k) | K120760 | LDR SPINE SPINETUNE TL SPINAL SYSTEM | MNH | 2012-06-27 | View |
| 510(k) | K113559 | LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS | ODP | 2011-12-29 | View |
No matching devices.
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