FDA 510(k) Applications Submitted by Anuja Yardi
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162752 | 09/30/2016 | ARTIA Reconstructive Tissue Matrix Perforated | LIFECELL CORPORATION |
| K213287 | 10/01/2021 | StageOne Knee Cement Spacer Molds | Biomet, Inc. |
| K163647 | 12/23/2016 | Revolve Envi 600 Advanced Adipose System | LifeCell Corporation |
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