FDA 510(k) Applications Submitted by RANDY THEKEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050058 | 01/11/2005 | THEKEN REVEAL VBR SYSTEM | THEKEN SURGICAL,LLC |
| K041592 | 06/14/2004 | CORAL SPINAL SYSTEM | THEKEN SURGICAL |
| K012278 | 07/19/2001 | THEKEN SMALL CEMENT RESTRICTOR | THEKEN SURGICAL,LLC |
| K012462 | 08/01/2001 | THEKEN LARGE CEMENT RESTRICTOR | THEKEN SURGICAL,LLC |
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