FDA 510(k) Applications Submitted by BRM Extremities Srl
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220142 | 01/18/2022 | BRM Digitalis Spacer | BRM Extremities Srl |
| K203773 | 12/23/2020 | BRM TOOL Screws | BRM Extremities Srl |
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