Trans1 Incorporated
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120991 | TRANS1 INTERBODY FUSION SYSTEM | MAX | 2012-08-23 | View |
| 510(k) | K102334 | TRANS1 AXIALIF PLUS | KWQ | 2011-03-14 | View |
| 510(k) | K100210 | TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T | MAX | 2010-08-26 | View |
| 510(k) | K092124 | AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II | KWQ | 2010-01-21 | View |
| 510(k) | K073643 | TRANS1 AXIALIF 2-LEVEL OR II SYSTEM | KWQ | 2008-04-28 | View |
| 510(k) | K073515 | TRANS1 FACET SCREW | MRW | 2008-03-11 | View |
| 510(k) | K073514 | TRANS1 AXIAL FIXATON SYSTEM | KWQ | 2008-01-11 | View |
| 510(k) | K051856 | TRANS1 FACET SCREWS | MRW | 2005-09-26 | View |
| 510(k) | K050965 | TRANS1 AXIALIF SYSTEM | KWQ | 2005-06-14 | View |
No matching devices.
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