FDA 510(k) Applications Submitted by restor3d
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231458 | 05/19/2023 | Extremity Staple | restor3d |
| K223326 | 10/31/2022 | Axiom PSR System | Restor3d |
| K211789 | 06/10/2021 | restor3d Pin Implants | restor3d |
| K193491 | 12/17/2019 | restor3d Metallic Interference Screw | restor3D |
| K220523 | 02/23/2022 | restor3d TiDAL Lumbar Interbody Fusion Device | Restor3d |
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