New Business Development, LLC
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) | K072029 | PHENIX VERTEBRAL BODY REPLACEMENT | MQP | 2007-10-15 | View |
| 510(k) | K050377 | NBD HEAD SCREW | HAW | 2005-04-07 | View |
| 510(k) | K032196 | NBD DISPOSABLE RF CANNULAE | GXI | 2003-10-09 | View |
| 510(k) | K021788 | NBD CEMENT RESTRICTOR DEVICE | JDK | 2002-10-04 | View |
No matching devices.
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