Verticor, Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K110047 | VERTICOR K-WIRE SYSTEM | HTY | 2011-02-28 | View |
| 510(k) | K103137 | VENUS ANTERIOR CERVICAL PLATE | KWQ | 2011-02-10 | View |
| 510(k) | K091426 | CERVICORE CORPECTOMY CAGE | MQP | 2009-12-23 | View |
No matching devices.
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