Musculoskeletal Clinical Regulatory Advisers
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| VU CPOD INTERVERTEBRAL BODU FUSION DEVICE (K101363) | Musculoskeletal Clinical Regulatory Advisers | 2010-12-16 |
Track Musculoskeletal Clinical Regulatory Advisers automatically
Every clearance here is in the API, with alerts when new ones post.