Dio Medical Co., Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| 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 |
| 510(k) | K122872 | INTERVERTEBRAL BODY FUSION DEVICE | ODP | 2013-02-28 | View |
| 510(k) | K121862 | REX ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2012-10-31 | View |
| 510(k) | K113324 | REXIOUS HOOK FIXATION SYSTEMS | KWP | 2012-03-28 | View |
| 510(k) | K111362 | REXIOUS SPINAL FIXATION SYSTEM | MNH | 2011-07-21 | View |
| 510(k) | K100765 | FIXPINE II SYSTEM | MNI | 2010-07-19 | View |
No matching devices.
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