FDA 510(k) Applications Submitted by Cindy Toyama
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230486 | 02/23/2023 | Cove Strip | SeaSpine Orthopedics Corporation |
| K231030 | 04/11/2023 | Cove Putty, OsteoCove Putty | SeaSpine Orthopedics Corporation |
| K232668 | 09/01/2023 | Cove Strip, OsteoCove Strip | SeaSpine Orthopedics Corporation |
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