Kenneth J. Hoek, M.D., Inc.
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| FEMORAL CEMENT REMOVAL INSTRUMENTS (K870217) | Kenneth J. Hoek, M.D., Inc. | 1987-02-06 |
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Every clearance here is in the API, with alerts when new ones post.