FDA 510(k) Applications Submitted by GALLINI MEDICAL DEVICES, SRL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K141557 | 06/12/2014 | HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - CERVICAL, HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - LUMBAR | GALLINI MEDICAL DEVICES, SRL |
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