FDA 510(k) Applications Submitted by Foundation Surgical Group, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241468 | 05/24/2024 | Vertiwedge« Intraosseous System | Foundation Surgical Group, Inc. |
| K241487 | 05/24/2024 | Interwedge« Standalone Lateral | Foundation Surgical Group, Inc. |
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