Gallini Medical Devices, Srl
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - CERVICAL, HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - LUMBAR (K141557) | Gallini Medical Devices, Srl | 2014-12-08 |
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Every clearance here is in the API, with alerts when new ones post.