Ldr Spine USA
FDA 510(k) & PMA Approved Devices — 23 products
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Total Devices23
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153495 | Avenue L Lateral Lumbar Cage, Avenue T TLIF Cage System, ROI-A ALIF Cage System, ROI-T Implant System | MAX | 2016-03-31 | View |
| 510(k) | K152137 | FacetBRIDGE System | MRW | 2016-01-25 | View |
| 510(k) | K110327 | LDR SPINE ROI-A INTERBODY FUSION SYSTEM | OVD | 2011-09-30 | View |
| 510(k) | K102331 | LDR SPINE USA SPINETUNE TL SPINAL SYSTEM | MNI | 2010-10-15 | View |
| 510(k) | K102265 | LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2010-09-29 | View |
| 510(k) | K100575 | LDR SPINE USA SPINE TUNE TL SPINE SYSTEM | MNI | 2010-03-31 | View |
| 510(k) | K091088 | LDR SPINE CERVICAL INTERBODY FUSION SYSTEM | ODP | 2009-07-14 | View |
| 510(k) | K090507 | MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM | MAX | 2009-06-25 | View |
| 510(k) | K083857 | LDR SPINE ROI-C IMPLANT | MQP | 2009-02-12 | View |
| 510(k) | K082262 | LDR SPINE ROI INTERBODY FUSION SYSTEM | MAX | 2009-02-02 | View |
| 510(k) | K082592 | LDR SPINE EASYSPINE SYSTEM | NKB | 2008-10-08 | View |
| 510(k) | K080728 | LDR SPINE ROI-C IMPLANT | MQP | 2008-05-29 | View |
| 510(k) | K080569 | LDR SPINE ROI-T IMPLANT | MQP | 2008-05-07 | View |
| 510(k) | K080572 | LDR SPINE ROI-A IMPLANT | MQP | 2008-04-07 | View |
| 510(k) | K072132 | LDR SPINE ROI-T SYSTEM | MQP | 2007-08-30 | View |
| 510(k) | K070341 | LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM | KWP | 2007-08-08 | View |
| 510(k) | K063794 | MODIFICATION TO EASYSPINE SYSTEM | MNI | 2007-01-24 | View |
| 510(k) | K061462 | BF+ (PH) | MQV | 2006-12-15 | View |
| 510(k) | K061017 | EASYSPINE SYSTEM | MNI | 2006-08-10 | View |
| 510(k) | K043479 | MC+ PARTIAL VBR | MQP | 2005-06-30 | View |
No matching devices.
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