FDA 510(k) Applications Submitted by CurvaFix, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180050 | 01/08/2018 | CurvaFix Intramedullary Rodscrew System | CurvaFix, Inc. |
| K222505 | 08/18/2022 | CurvaFix IM System | CurvaFix, Inc. |
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