FDA 510(k) Applications Submitted by JAMES BURROWS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070341 | 02/06/2007 | LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM | LDR SPINE USA |
| K072132 | 08/02/2007 | LDR SPINE ROI-T SYSTEM | LDR SPINE USA |
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