FDA 510(k) Applications Submitted by GLW, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221489 | 05/23/2022 | Artemis Proximal Femoral Nail System | GLW, Inc. |
| K201379 | 05/26/2020 | Artemis Proximal Femoral Nail System | GLW, Inc. |
| K223847 | 12/22/2022 | CREEDÖ Cannulated Screws | GLW, Inc. |
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