Custom Spine, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120597 | KOMPREDA | MRW | 2013-05-03 | View |
| 510(k) | K111726 | PATHWAY AVID | MAX | 2012-02-06 | View |
| 510(k) | K111099 | ISSYS LP SPINAL FIXATION SYSTEM | NKB | 2011-05-05 | View |
| 510(k) | K092904 | PATHWAY IVB/VBR | ODP | 2009-12-22 | View |
| 510(k) | K091134 | CUSTOM SPINE REGENT ANTERIOR CERVICAL PLATE | KWQ | 2009-08-17 | View |
| 510(k) | K090566 | PATHWAY AVID | MAX | 2009-06-01 | View |
| 510(k) | K080281 | PATHWAY | MAX | 2008-05-01 | View |
| 510(k) | K072866 | ISSYS LP SPINAL FIXATION SYSTEM | KWP | 2007-12-13 | View |
| 510(k) | K070281 | ISSYS LP SPINAL FIXATION SYSTEM | NKB | 2007-06-11 | View |
| 510(k) | K043522 | ISSYS PEDICLE SCREW SYSTEM | KWP | 2005-01-14 | View |
No matching devices.
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