FDA 510(k) Applications Submitted by Caryn Sailor
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200290 | 02/05/2020 | Resorbable Mesh Pouch (Ballast MT, OsteoBallast MT) | SeaSpine Orthopedics Corporation |
| K212135 | 07/08/2021 | Dry DBM- A Putty | SeaSpine Corporation |
| K193040 | 10/31/2019 | Resorbable Mesh Device | SeaSpine Orthopedics Corporation |
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