FDA 510(k) Applications Submitted by Synovis Life Technologies. Inc. (A Subsidiary Of Baxter
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K213125 | 09/27/2021 | PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology | Synovis Life Technologies. Inc. (A Subsidiary Of Baxter |
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