Dio Medical Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-02-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162849 | Huvex Interspinous Fixation System | PEK | 2017-02-16 | View |
| 510(k) | K162220 | DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage | ODP | 2016-11-21 | View |
No matching devices.