FDA 510(k) Applications Submitted by Additive Device, Inc. (ADI) d/b/a restor3d
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191047 | 04/19/2019 | ADI TiDAL Osteotomy Wedge | Additive Device, Inc. (ADI) d/b/a restor3d |
| K191812 | 07/05/2019 | ADI Cervical Interbody Fusion Device | Additive Device, Inc. (ADI) d/b/a restor3d |
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