FDA 510(k) Applications Submitted by RootLoc Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170753 | 03/13/2017 | Acculoc Total Knee System | RootLoc Co., Ltd. |
| K182370 | 08/31/2018 | Acculoc Total Knee System | RootLoc Co., Ltd. |
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