FDA 510(k) Applications Submitted by KIERSTEN SODERMAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120760 | 03/13/2012 | LDR SPINE SPINETUNE TL SPINAL SYSTEM | LDR SPINE USA INC. |
| K113559 | 12/01/2011 | LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS | LDR SPINE USA INC. |
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