Foundation Surgical Group, Inc.
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Foundation Surgical Navigated Lateral Disc Prep Instruments (K260011) | Foundation Surgical Group, Inc. | 2026-04-16 |
| Vertiwedge® Intraosseous System (K241468) | Foundation Surgical Group, Inc. | 2024-11-07 |
| Interwedge® Standalone Lateral (K241487) | Foundation Surgical Group, Inc. | 2024-10-02 |
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Every clearance here is in the API, with alerts when new ones post.