FDA 510(k) Applications Submitted by VERTICOR, LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110047 | 01/06/2011 | VERTICOR K-WIRE SYSTEM | VERTICOR, LTD |
| K091426 | 05/13/2009 | CERVICORE CORPECTOMY CAGE | VERTICOR, LTD |
| K103137 | 10/25/2010 | VENUS ANTERIOR CERVICAL PLATE | VERTICOR, LTD |
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