FDA 510(k) Applications Submitted by MANAS M LELE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161370 | 05/17/2016 | Durepair Dura Regeneration Matrix | Medtronic Neurosurgery |
| K131101 | 04/19/2013 | ITERO SOFTWARE | CADENT, LTD. AN ALIGN TECHNOLOGY COMPANY |
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