Lanx, Inc.
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) | K131547 | LANX FUSION SYSTEM | OVD | 2013-07-12 | View |
| 510(k) | K131156 | LANX SPINAL FIXATION SYSTEM | KWP | 2013-05-24 | View |
| 510(k) | K123767 | LANX FUSION SYSTEM- SA | OVD | 2013-03-18 | View |
| 510(k) | K121316 | LANX SPINAL FIZATION SYSTEM | NKB | 2012-09-10 | View |
| 510(k) | K122145 | LANX SPINAL FIXATION SYSTEM | NKB | 2012-08-17 | View |
| 510(k) | K121940 | LANX SPINAL FIXATION SYSTEM | NKB | 2012-08-02 | View |
| 510(k) | K113434 | LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS) | NKB | 2011-12-19 | View |
| 510(k) | K112388 | LANX CERVICAL SA | OVE | 2011-12-16 | View |
| 510(k) | K103091 | LANX SPINAL FIXATION SYSTEM | KWP | 2011-04-15 | View |
| 510(k) | K103237 | LANX SPINAL SYSTEM | NKB | 2011-03-25 | View |
| 510(k) | K103666 | LANX LATERAL | MAX | 2011-03-23 | View |
| 510(k) | K103660 | LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM | ODP | 2011-02-28 | View |
| 510(k) | K100888 | MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM | KWP | 2010-11-15 | View |
| 510(k) | K101364 | LANX FACET SCREW SYSTEM | MRW | 2010-08-16 | View |
| 510(k) | K100935 | LANX SPINAL FIXATION SYSTEM | NKB | 2010-08-06 | View |
| 510(k) | K100191 | LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS) | KWP | 2010-04-15 | View |
| 510(k) | K092765 | LANX ANTERIOR PLATING SYSTEM | KWQ | 2010-04-07 | View |
| 510(k) | K092656 | LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM | KWP | 2009-11-24 | View |
| 510(k) | K092536 | SPINAL FIXATION SYSTEM | NKB | 2009-10-30 | View |
| 510(k) | K083815 | LANX FUSION SYSTEM | MAX | 2009-04-20 | View |
No matching devices.
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