FDA 510(k) Applications Submitted by SANACOR
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090477 | 02/24/2009 | ALPINE PEDICLE SCREW SYSTEM | SANACOR |
| K070933 | 04/03/2007 | LOWTOP PEDICLE SCREW SYSTEM | SANACOR |
| K073500 | 12/13/2007 | ACTIVE ANTERIOR CERVICAL PLATE SYSTEM | SANACOR |
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