Theken Surgical,Llc
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K050058 | THEKEN REVEAL VBR SYSTEM | MQP | 2005-05-17 | View |
| 510(k) | K032064 | THEKEN CPOD/LPOD VERTEBRAL BODY REPLACEMENT SYSTEM | MQP | 2004-02-20 | View |
| 510(k) | K012462 | THEKEN LARGE CEMENT RESTRICTOR | JDK | 2001-10-29 | View |
| 510(k) | K012278 | THEKEN SMALL CEMENT RESTRICTOR | JDK | 2001-10-17 | View |
| 510(k) | K010466 | TETHER ACFS | KWQ | 2001-05-16 | View |
| 510(k) | K983622 | BODYFORM THORACO-LUMBAR FIXATION SYSTEM | KWQ | 1998-12-30 | View |
No matching devices.
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