Amedica Corp.
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173453 | Valeo® C+CSC with Lumen Interbody Fusion Device | ODP | 2018-03-05 | View |
| 510(k) | K161405 | Valeo II Interbody Fusion Device System | MAX | 2016-08-19 | View |
| 510(k) | K121892 | PHANTOM PLUS CERAMIC CAGE SYSTEM | MAX | 2012-08-24 | View |
| 510(k) | K091278 | VALEO SPACER SYSTEM | MAX | 2010-01-28 | View |
| 510(k) | K082037 | SEEPLATE CERVICAL PLATE SYSTEM | KWQ | 2008-09-26 | View |
| 510(k) | K073430 | VALEO PEDICLE SCREW SPINAL SYSTEM | NKB | 2008-01-29 | View |
| 510(k) | K073505 | MODIFICATION TO VALEO VBR | MQP | 2008-01-09 | View |
| 510(k) | K073125 | VALEO VBR | MQP | 2007-12-05 | View |
| 510(k) | K072022 | VALEO PEDICLE SCREW SPINAL SYSTEM | NKB | 2007-11-19 | View |
| 510(k) | K071990 | VALEO CERVICAL PLATE SYSTEM | KWQ | 2007-10-29 | View |
| 510(k) | K051525 | ARX SPINAL SYSTEM | MQP | 2006-02-17 | View |
| 510(k) | K050699 | MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004 | JDK | 2005-04-15 | View |
| 510(k) | K022729 | VENTED CEMENT RESTRICTOR | JDX | 2002-11-14 | View |
No matching devices.
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