FDA 510(k) Applications Submitted by Paragon 28 Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231231 | 04/28/2023 | MR Safety and Compatibility Testing and Labeling for Paragon 28 Orthopedic Fixation Devices | Paragon 28 Inc. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact