Advanced Medical Technologies AG
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) | K121330 | WAVE O CAGE | MAX | 2012-06-29 | View |
| 510(k) | K121333 | WAVE D CAGE | MAX | 2012-06-29 | View |
| 510(k) | K121332 | LOOP CAGE | MAX | 2012-06-29 | View |
| 510(k) | K121288 | FUSE CAGE | MAX | 2012-06-29 | View |
| 510(k) | K100945 | FUSE PLIF CAFE | MAX | 2011-02-09 | View |
| 510(k) | K080401 | SHELL CAGE, WAVE CAGE, LOOP CAGE | MAX | 2008-05-09 | View |
| 510(k) | K033148 | ART ANTERIOR SPINAL SYSTEM | KWQ | 2004-04-12 | View |
| 510(k) | K033150 | ART POSTERIOR SPINAL SYSTEM | MNI | 2004-03-01 | View |
No matching devices.
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