Bk Meditech, Co., Ltd.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200981 | Mega Plus MIS Spine System | NKB | 2020-08-11 | View |
| 510(k) | K183080 | Mega Plus Spine System | NKB | 2018-12-10 | View |
| 510(k) | K173180 | Mega Plus Spine System | NKB | 2018-03-15 | View |
| 510(k) | K120464 | INNESIS PEEK CAGE | MAX | 2013-01-18 | View |
| 510(k) | K110426 | DYNA-EXTOR II | KTT | 2011-11-02 | View |
| 510(k) | K090424 | DVX SPINE SYSTEM | MNH | 2009-05-14 | View |
| 510(k) | K080876 | DVX SPINE SYSTEM | MNH | 2008-06-04 | View |
| 510(k) | K072436 | MEGA SPINE SYSTEM | MNI | 2007-11-01 | View |
| 510(k) | K061599 | PIN SCREW | JDW | 2006-07-26 | View |
No matching devices.
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