Advanced Spine Technology, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K062686 | UNIVERSAL SPINAL ANTERIOR LOCKING PLATE SYSTEM | KWQ | 2006-10-05 | View |
| 510(k) | K993066 | WINDOW CERVICAL DYNAMIC PLATE SYSTEM | KWQ | 2000-06-07 | View |
| 510(k) | K992147 | TRIPLE-FIX SPINAL FIXATION SYSTEM | MNI | 2000-02-28 | View |
| 510(k) | K951266 | AMSET R-F SYSTEM | MNH | 1995-11-21 | View |
No matching devices.
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