FDA 510(k) Applications Submitted by POINTNIX CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222738 | 09/09/2022 | Point implant system | PointNix Co., Ltd |
| K121800 | 06/19/2012 | POINT 500 HD POINT500C HD | POINTNIX CO., LTD |
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