Aesculap Implants Systems, Inc.
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Modulift Vertebral Body Replacement (VBR) System (K172032) | Aesculap Implants Systems, Inc. | 2017-11-20 |
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Every clearance here is in the API, with alerts when new ones post.