AgNovos Healthcare USA, LLC
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K181585 | JGH1 Core Deccompression Procedure Kit | MQV | 2018-07-20 | View |
| 510(k) | K181342 | JGH1 Bone Graft Substitute | MQV | 2018-07-19 | View |
No matching devices.
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